No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 30381780125826 | DFUSTAPLERKIT | DFUSTAPLERKIT | Box of 3 Disposable Skin Staplers | GDT,GAG | Staple, Removable (Skin),Stapler, Surgical | NA | |
2 | 20705031132914 | 44152 | BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms. | FRO | Dressing, wound, drug | BioPatch™ | ||
3 | 20705031132907 | 44151 | BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms. | FRO | Dressing, wound, drug | BioPatch™ | ||
4 | 20705031132891 | 44150 | BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms. | FRO | Dressing, wound, drug | BioPatch™ | ||
5 | 20705031004358 | 3152 | BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms. | FRO | Dressing, wound, drug | BioPatch™ | ||
6 | 20705031004341 | 3151 | BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms. | FRO | Dressing, wound, drug | BioPatch™ | ||
7 | 20705031004334 | 3150 | BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic BioPatch™ Antimicrobial Dressing with Chlorhexidine Gluconate is a hydrophillic polyurethane absorptive foam with Chlorhexidine Gluconate (CHG) which inhibits bacterial growth under the dressing. The dressing is intended to be used to absorb exudate, cover a wound caused by vascular and nonvascular percutaneous medical devices during surgery, as well as reduce local infection and colonization of microorganisms. | FRO | Dressing, wound, drug | BioPatch™ | ||
8 | 10381780490036 | WD62202 | WD62202 | creos™ xenoplug Absorbable Collagen Wound Dressing for Dental Surgery | LPG | MATERIAL, DRESSING, SURGICAL, POLYLACTIC ACID | creos™ | |
9 | 10381780490029 | WD62201 | WD62201 | creos™ xenocote Absorbable Collagen Wound Dressing for Dental Surgery | LPG | MATERIAL, DRESSING, SURGICAL, POLYLACTIC ACID | creos™ | |
10 | 10381780490012 | WD62200 | WD62200 | creos™ xenotape Absorbable Collagen Wound Dressing for Dental Surgery | LPG | MATERIAL, DRESSING, SURGICAL, POLYLACTIC ACID | creos™ | |
11 | 10381780211082 | NL850500V | NL850500V | Integra™ Ventricular Drainage System provides a sterile path for the drainage of Integra™ Ventricular Drainage System provides a sterile path for the drainage of cerebrospinal fluid (CSF) from an intraventricular catheter to a collection bag. The system can be used for external drainage, and the management of hydrocephalic shunt infections, or treatment of other cerebral conditions such as pre-operative or post-operative pressure monitoring of CSF to control increased intracranial pressure. | JXG | Shunt, central nervous system and components | 2 | N/A |
12 | 10381780114369 | TXG10 | TXG10 | Trel-X™Gel, 10cc is human bone that has been demineralized and combined with po Trel-X™Gel, 10cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package. | MQV | FILLER, BONE VOID, CALCIUM COMPOUND | 2 | Trel-X Gel |
13 | 10381780112525 | XPRES105 | XPRES105 | Trel-XPress 100, 5cc is made using demineralized human bone mixed with poloxamer Trel-XPress 100, 5cc is made using demineralized human bone mixed with poloxamer reverse phase medium. Trel-XPress 100 is formulated into a putty form and is provided in a sterile, single use package. | MQV,MBP | FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human growth factor) | 2 | Trel X-Press 100 |
14 | 10381780112532 | XPRES125 | XPRES125 | Trel-XPress 100, 2.5cc is made using demineralized human bone mixed with poloxam Trel-XPress 100, 2.5cc is made using demineralized human bone mixed with poloxamer reverse phase medium. Trel-XPress 100 is formulated into a putty form and is provided in a sterile, single use package. | MQV,MBP | FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human growth factor) | 2 | Trel X-Press 100 |
15 | 10381780112518 | XPRES110 | XPRES110 | Trel-XPress 100, 10cc is made using demineralized human bone mixed with poloxame Trel-XPress 100, 10cc is made using demineralized human bone mixed with poloxamer reverse phase medium. Trel-XPress 100 is formulated into a putty form and is provided in a sterile, single use package. | MQV,MBP | FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human FILLER, BONE VOID, CALCIUM COMPOUND,Filler, bone void, osteoinduction (w/o human growth factor) | 2 | Trel X-Press 100 |
16 | 10381780112501 | TXG05 | TXG05 | Trel-X™Gel, 5cc is human bone that has been demineralized and combined with pol Trel-X™Gel, 5cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package. | MQV | FILLER, BONE VOID, CALCIUM COMPOUND | 2 | Trel-X Gel |
17 | 10381780112495 | TXG01 | TXG01 | Trel-X™Gel, 1cc is human bone that has been demineralized and combined with pol Trel-X™Gel, 1cc is human bone that has been demineralized and combined with poloxamer reverse phase medium which is formulated into a gel or putty-like form. Trel-X is provided in a sterile, single patient use package. | MQV | FILLER, BONE VOID, CALCIUM COMPOUND | 2 | Trel-X Gel |
18 | 10381780112266 | INS410MM | INS410MM | The Evolution Pole Mount Assembly provides support and alignment for the Externa The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
19 | 10381780112259 | INS410CM | INS410CM | The Evolution Pole Mount Assembly provides support and alignment for the Externa The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
20 | 10381780112242 | INS410 | INS410 | The Evolution Pole Mount Assembly provides support and alignment for the Externa The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
21 | 10381780112228 | INS400L | INS400L | The Pole Mount Laser Level device is provided with mounting bracket for use with The Pole Mount Laser Level device is provided with mounting bracket for use with Integra Pole Mount Assemblies. The Pole Mount Laser provides alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular catheter or lumbar catheter to an external ventricular drainage system. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
22 | 10381780112211 | INS400CM | INS400CM | The Evolution Pole Mount Assembly provides support and alignment for the Externa The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
23 | 10381780112204 | INS400 | INS400 | The Evolution Pole Mount Assembly provides support and alignment for the Externa The Evolution Pole Mount Assembly provides support and alignment for the External CSF Drainage and Monitoring Systems. These systems are used for draining CSF from an intraventricular or lumbar catheter to an external CSF drainage system. This Integra Pole Mount is provided with a laser leveling device and an optional line level. The laser level is attached via a bracket. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
24 | 10381780072515 | NL97001S01 | NL97001S01 | STERILE LUER CONNECTOR | JXG | Shunt, central nervous system and components | N/A | |
25 | 10381780072294 | NL8501222 | NL8501222 | The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of C The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of CSF in children with small veins. The distal section of the catheter is reduced to approximately one-half standard diameter for easier insertion. The proximal section of the catheter contains an imbedded barium sulfate-impregnated strip, and the distal section is fully barium sulfate-impregnated. The infant model does not contain graduation markets. | JXG | Shunt, central nervous system and components | Integra Pudenz Infant Cardiac Catheter | |
26 | 10381780072287 | NL8501221 | NL8501221 | The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of C The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of CSF in children with small veins. The distal section of the catheter is reduced to approximately one-half standard diameter for easier insertion. The proximal section of the catheter contains an imbedded barium sulfate-impregnated strip, and the distal section is fully barium sulfate-impregnated. The infant model does not contain graduation markets. | JXG | Shunt, central nervous system and components | Integra Pudenz Infant Cardiac Catheter | |
27 | 10381780071815 | NW720 | NW720 | NEURAWRAP 7MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable coll NEURAWRAP 7MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
28 | 10381780071808 | NW1020 | NW1020 | NEURAWRAP 10MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable col NEURAWRAP 10MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
29 | 10381780071709 | NL8508601 | NL8508601 | The External CSF Drainage Systems provide a sterile fluid path resistant to micr The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. The systems are used to drain CSF from ventricles of the brain or the lumbar subarachnoid space to a drainage bag. System components facilitate CSF drainage, fluid injection, CSF sampling and intracranial pressure monitoring. | JXG | Shunt, central nervous system and components | Integra™ External Drainage System | |
30 | 10381780071693 | NL8508600 | NL8508600 | The External CSF Drainage Systems provide a sterile fluid path resistant to micr The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. The systems are used to drain CSF from ventricles of the brain or the lumbar subarachnoid space to a drainage bag. System components facilitate CSF drainage, fluid injection, CSF sampling and intracranial pressure monitoring. | JXG | Shunt, central nervous system and components | Integra™ External Drainage System | |
31 | 10381780071679 | NL8508501 | NL8508501 | The Allegheny EVD System provides a sterile fluid path for the drainage of CSF f The Allegheny EVD System provides a sterile fluid path for the drainage of CSF from an intraventricular catheter to a drainage bag. System components facilitate ventricular drainage, fluid injection, CSF sampling and intracranial pressure monitoring. | JXG | Shunt, central nervous system and components | Integra ™ NeuroSciences Allegheny EVD System | |
32 | 10381780071129 | INS9030 | INS9030 | LIMITORR 30 MLVolume Limiting External CSF Drainage System with 20ml Burette.Lim LIMITORR 30 MLVolume Limiting External CSF Drainage System with 20ml Burette.LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of cerebrospinal fluid (CSF) from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage System was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSFdrainage. The burette in the Volume Limiting External CSF Drainage System contains a volume limiting valve which stops drainage when the pre-determined volume (20ml or 30ml) is reached. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
33 | 10381780071273 | NL8500132 | NL8500132 | Multi-Purpose Valve, Model: High Pressure 95-150mm H20 closing pressure | JXG | Shunt, central nervous system and components | 2 | N/A |
34 | 10381780071136 | INS9030SP1 | INS9030SP1 | The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provide The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of CSF from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage system was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSF drainage. The burette contains a volume limiting valve which stops drainage when the pre-determine volume (20ml or 30ml) is reached. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
35 | 10381780071112 | INS9020SP1 | INS9020SP1 | The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provide The LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of CSF from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage system was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSF drainage. The burette contains a volume limiting valve which stops drainage when the pre-determine volume (20ml or 30ml) is reached. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
36 | 10381780071105 | INS9020 | INS9020 | LIMITORR 20 MLVolume Limiting External CSF Drainage System with 20ml Burette.Lim LIMITORR 20 MLVolume Limiting External CSF Drainage System with 20ml Burette.LimiTorr Volume Limiting External CSF Drainage and Monitoring System provides a closed system for the drainage of cerebrospinal fluid (CSF) from the ventricles of the brain or the lumbar subarachnoid space to an external drainage bag. The LimiTorr Volume Limiting External CSF Drainage System was designed to include a volume limiting valve mechanism which reduces the chances for excessive CSFdrainage. The burette in the Volume Limiting External CSF Drainage System contains a volume limiting valve which stops drainage when the pre-determined volume (20ml or 30ml) is reached. | JXG | Shunt, central nervous system and components | LimiTorr™ | |
37 | 10381780038535 | 62208 | 62208 | HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks. | LYC | Bone grafting material, synthetic | HeliMend® Advanced | |
38 | 10381780038528 | 62207 | 62207 | HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purif HeliMEND and HeliMEND Advanced absorbable collagen membranes are made from purified bovine tendon. These collagen products provide wound stabilization and create space during guided tissue regeneration procedures where a longer absorption rate is desired. HeliMEND Advanced collagen membrane is absorbed within 18 weeks. | LYC | Bone grafting material, synthetic | HeliMend® Advanced | |
39 | 10381780026457 | NW740 | NW740 | NEURAWRAP 7MM 4CM NERVE PROTECTOR The NeuraWrap Nerve Protector is an absorbable NEURAWRAP 7MM 4CM NERVE PROTECTOR The NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap Nerve Protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap Nerve Protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap Nerve Protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
40 | 10381780026440 | NW540 | NW540 | NEURAWRAP 5MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbab NEURAWRAP 5MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
41 | 10381780026433 | NW520 | NW520 | NEURAWRAP 5MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable coll NEURAWRAP 5MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
42 | 10381780026426 | NW340 | NW340 | NEURAWRAP 3MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbabl NEURAWRAP 3MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
43 | 10381780026419 | NW320 | NW320 | NEURAWRAP 3MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable coll NEURAWRAP 3MM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
44 | 10381780026402 | NW1040 | NW1040 | NEURAWRAP 10MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbab NEURAWRAP 10MM X 4CM NERVE PROTECTORThe NeuraWrap Nerve Protector is an absorbable collagen implant that provides a non-constricting encasement for injured peripheral nerves for protection of the neural environment. It is designed to be an interface between the nerve and the surrounding tissue. When hydrated, the NeuraWrap nerve protector is an easy to handle, soft, pliable, nonfriable, porous collagen conduit. The wall of the conduit has a longitudinal slit that allows NeuraWrap nerve protector to be spread open for easy placement over the injured nerve. The resilience of the collagen conduit allows NeuraWrap nerve protector to recover and maintain closure once the device is placed around the nerve. | JXI | CUFF, NERVE | NeuraWrap™ | |
45 | 10381780024255 | NL8501220 | NL8501220 | The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of C The Infant Cardiac Catheter model is designed for ventriculoatrial shunting of CSF in children with small veins. The distal section of the catheter is reduced to approximately one-half standard diameter for easier insertion. The proximal section of the catheter contains an imbedded barium sulfate-impregnated strip, and the distal section is fully barium sulfate-impregnated. The infant model does not contain graduation markets. | JXG | Shunt, central nervous system and components | Integra Pudenz Infant Cardiac Catheter | |
46 | 10381780023388 | AirSpray01 | AirSpray01 | AIR ASSISTED SPRAYER, ONE UNIT PER BOX | GCJ | Laparoscope, General & Plastic Surgery | 2 | Air Assisted Sprayer |
47 | 10381780000280 | 62-200 | 62-200 | HeliTape ® ABSORBABLE COLLAGEN Wound Dressing, 1in x 3in | LPG | Material, Dressing, Surgical, Polylactic Acid | HeliTape® | |
48 | 10381780114321 | RNFMTX0510 | RNFMTX0510 | Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for use in the reconstruction of soft tissue deficiencies. | FTM | Mesh, Surgical | 2 | Integra Reinforcement Matrix |
49 | 10381780114314 | RNFMTX0407 | RNFMTX0407 | Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for Integra Reinforcement Matrix is an acellular, sterile, porcine dermal matrix for use in the reconstruction of soft tissue deficiencies. | FTM | Mesh, Surgical | 2 | Integra Reinforcement Matrix |
50 | 10381780072409 | NL8508420 | NL8508420 | TRAUMACATH VENTRICULAR CATHETER SETThe TraumaCath Ventricular Catheter set cathe TRAUMACATH VENTRICULAR CATHETER SETThe TraumaCath Ventricular Catheter set catheter is barium striped. Designed for diverting fluid from the ventricles through a series of drainage holes, the catheter can be inserted into the ventricular cavity with the stainless steel stylet. A trocar is supplied with the catheter to facilitate subcutaneous tunneling away from the burr hole. The external portion of the catheter may be secured to the scalp by the suture tab. The luer lock supplied with each ventricular catheter set will connect the catheter to any Integra external drainage system. | JXG | Shunt, central nervous system and components | TraumaCath Ventricular Catheter Set |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00889024205567 | 76-6036 | CarriGen ® | ETEX CORPORATION | ||
2 | 00889024205550 | 76-6041 | EquivaBone ® | ETEX CORPORATION | ||
3 | 00889024205543 | 76-6022 | EquivaBone ® | ETEX CORPORATION | ||
4 | 00889024205536 | 76-6021 | EquivaBone ® | ETEX CORPORATION | ||
5 | 00889024205529 | 76-6027 | EquivaBone ® | ETEX CORPORATION | ||
6 | 00889024205512 | 76-6016 | Beta-bsm ® | ETEX CORPORATION | ||
7 | 00889024205505 | 76-6025 | Beta-bsm ® | ETEX CORPORATION | ||
8 | 00889024205499 | 76-6040 | Gamma-bsm ® | ETEX CORPORATION | ||
9 | 00889024205482 | 76-6010 | Gamma-bsm ® | ETEX CORPORATION | ||
10 | 00889024205475 | 76-6005 | Gamma-bsm ® | ETEX CORPORATION | ||
11 | 00889024205468 | 76-6023 | Gamma-bsm ® | ETEX CORPORATION | ||
12 | 00889024205451 | 76-6001 | Gamma-bsm ® | ETEX CORPORATION | ||
13 | ECURS20M1000 | 1000-2000µm | 5 x 2.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
14 | ECURS20M0500 | 500-1000µm | 5 x 2.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
15 | ECURS20M0150 | 150-500µm | 5 x 2.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
16 | ECURS10V0500 | 500-1000µm | 1 x 1.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
17 | ECURS10M1000 | 1000-2000µm | 5 x 1.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
18 | ECURS10M0500 | 500-1000µm | 5 x 1.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
19 | ECURS10M0150 | 150-500µm | 5 x 1.0 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
20 | ECURS05V0500 | 500-1000µm | 1 x 0.5 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
21 | ECURS05M1000 | 1000-2000µm | 5 x 0.5 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
22 | ECURS05M0500 | 500-1000µm | 5 x 0.5 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
23 | ECURS05M0150 | 150-500µm | 5 x 0.5 cc | Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recomm Device Name: CERASORB® M DENTALlndications for Use:CERASORB® M DENTAL is recommended for:- Augmentation or reconstructive treatment of the alveolar ridge- Filling of infrabony periodontal defects- Filling of defects after root resection, apicoectomy and cystectomy- Filling of extraction sockets to enhance preservation of the alveolar ridge- Elevation of the maxillary sinus floor- Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)- Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration (GBR) | Cerasorb M Dental | CURASAN AG |
24 | ECURL20V1000 | 1000-2000µm | 1 x 2.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
25 | ECURL20V0250 | 250-1000µm | 1 x 2.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
26 | ECURL20M1000 | 1000-2000µm | 5 x 2.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
27 | ECURL20M0250 | 250-1000µm | 5x2.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
28 | ECURL10V1000 | 1000-2000µm | 1 x 1.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
29 | ECURL10V0250 | 250-1000µm | 1 x 1.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
30 | ECURL10M1000 | 1000-2000µm | 5 x 1.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
31 | ECURL10M0250 | 250-1000µm | 5 x 1.0 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
32 | ECURL05V1000 | 1000-2000µm | 1 x 0.5 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
33 | ECURL05V0250 | 250-1000µm | 1 x 0.5 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
34 | ECURL05M1000 | 1000-2000µm | 5 x 0.5 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
35 | ECURL05M0250 | 250-1000µm | 5 x 0.5 cc | Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is i Device Name: Curasan OSSEOLIVE® DENTALlndications for Use:OSSEOLIVE® DENTAL is indicated for applications in oral andmaxillofacial surgery and dentistry, including filling and/or reconstruction of multi-walled(artificial or degenerative) bone defects, e.g.:- Defects after the extirpation of bone cysts- Augmentation of an atrophied alveolar ridge- Sinus lift or sinus floor elevation (subantral augmentation)- Filling of alveolar defects after tooth extraction for preservation of the alveolar ridge- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled bone pockets as well as the bi- and trifurcation defects- Defects after operative removal of retained teeth or corrective osteotomies | Osseolive Dental | CURASAN AG |
36 | ECURH20V0250 | 250-1000µm | 1 x 2.0 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
37 | ECURH20M1000 | 1000-2000µm | 1 x 2.0 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
38 | ECURH10V1000 | 1000-2000µm | 1 x 1.0 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
39 | ECURH10V0250 | 250-1000µm | 1 x 1.0 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
40 | ECURH10M1000 | 1000-2000µm | 5 x 1.0 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
41 | ECURH10M0250 | 250-1000µm | 5 x 1.0 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
42 | ECURH05V1000 | 1000-2000µm | 1 x 0.5 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
43 | ECURH05V0250 | 250-1000µm | 1 x 0.5 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
44 | ECURH05M1000 | 1000-2000µm | 5 x 0.5 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for t Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
45 | ECURH05M0250 | 250-1000µm | 5 x 0.5 cc | Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for Device Name: OSBONE® DENTALlndications for Use:OSBONE® DENTAL is intended for the filling and reconstruction of multi-walled bone defects, e.g.:- Defects after removal of bone cysts- Augmentation of the atrophied alveolar ridge- Sinus lift and sinus floor elevation (subantral augmentation)- Filling of alveolar defects following tooth extraction for alveolar ridge preservation- Filling of extraction defects to create an implant bed- Filling of two- or multi-walled infrabony pockets, and bi- and trifurcation defects- Support function for a membrane in controlled tissue regeneration (CTR)- Defects after surgical removal of retained teeth or corrective osteotomies- Other multi-walled bone defects of the alveolar processes | Osbone Dental | CURASAN AG |
46 | EALGA01000310C2 | A01000310C | A01000310C | algisorb™ | ALGOSS BIOTECHNOLOGIES GMBH | |
47 | EALGA01000310B2 | A01000310B | A01000310B | algisorb™ | ALGOSS BIOTECHNOLOGIES GMBH | |
48 | EALGA01000310A2 | A01000310A | A01000310A | algisorb™ | ALGOSS BIOTECHNOLOGIES GMBH | |
49 | 00856509002812 | 04-005-01-RGP | 04-005-01-RGP | Synthetic bone graft substitute in particulate form composed of beta-tricalcium Synthetic bone graft substitute in particulate form composed of beta-tricalcium phosphate indicated for use as a bone grafting material to fill, augment, or reconstruct periodontal or oral/maxillofacial defects that are surgically created osseous defects or osseous defects created from traumatic injury to the bone. | RegenPerio Dental Beta-TCP | CYTOPHIL, INC. |
50 | 00855286006082 | OG-SYR | OsteoGen Bioactive Resorbable Calcium Apatite Crystals | OsteoGen Pre-Filled Syringe - 0.3g / 0.6cc | IMPLADENT, LTD. |