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 | 10381780038511 | 62206 | 62206 | 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 | |
40 | 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™ | |
41 | 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™ | |
42 | 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™ | |
43 | 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™ | |
44 | 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™ | |
45 | 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™ | |
46 | 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 | |
47 | 10381780023388 | AirSpray01 | AirSpray01 | AIR ASSISTED SPRAYER, ONE UNIT PER BOX | GCJ | Laparoscope, General & Plastic Surgery | 2 | Air Assisted Sprayer |
48 | 10381780000280 | 62-200 | 62-200 | HeliTape ® ABSORBABLE COLLAGEN Wound Dressing, 1in x 3in | LPG | Material, Dressing, Surgical, Polylactic Acid | HeliTape® | |
49 | 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 |
50 | 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 |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 07610221071913 | 501058 | Wound Matrix PLUS | GEISTLICH PHARMA AG | ||
2 | 07610221071906 | 501057 | Wound Matrix PLUS | GEISTLICH PHARMA AG | ||
3 | 07610221013227 | 500480 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
4 | 07610221013210 | 500479 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
5 | 07610221013203 | 500478 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
6 | 07610221013197 | 500477 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
7 | 07610221013180 | 500476 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
8 | 07610221013173 | 500475 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
9 | 07610221013166 | 500474 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
10 | 07610221012626 | 500427 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
11 | 07610221012619 | 500426 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
12 | 07610221012602 | 500425 | Geistlich Derma-Gide™ | GEISTLICH PHARMA AG | ||
13 | 07290108991307 | 4B-T0010 | MIS 4Bone Tape Resorbable Collagen Tape | MIS 4BONE | MIS IMPLANTS TECHNOLOGIES LTD. | |
14 | 07290108991246 | 4B-P0010 | MIS 4Bone Plug Resorbable Collagen Plug | MIS 4BONE | MIS IMPLANTS TECHNOLOGIES LTD. | |
15 | 05694310963930 | Micro 114 sq cm | 50202P32D0D | Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indica Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indicated for the management of wounds including: Partial and full thickness wounds, Trauma wounds including second degree burns, Surgical wounds including donor sites/ grafts.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-graftguide/ | Kerecis® Omega3 GraftGuide™ | KERECIS HF. |
16 | 05694310963916 | Micro 95 sq cm | 50205P31D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
17 | 05694310963893 | 6x8 cm | 50205S18D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
18 | 05694310963879 | 4x6 cm Meshed 2:1 | 50205N20D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
19 | 05694310963855 | 4x6 cm | 50205S20D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
20 | 05694310963831 | 6x8 cm Meshed 2:1 | 50205N18D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
21 | 05694310963770 | 30 mm Circular | 50215I52B0D | Bilayer wound management medical device product made from fish skin and silicone Bilayer wound management medical device product made from fish skin and silicone. Kerecis® Omega3 MariGen® Shield is indicated for the management of wounds including: Partial and full-thickness wounds, Pressure ulcers, Venous ulcers, Chronic vascular ulcers, Diabetic ulcers, Trauma wounds (abrasions, lacerations, partial-thickness burns, skin tears), Surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and Draining wounds. https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen-shield/ | Kerecis® Omega3 MariGen® Shield | KERECIS HF. |
22 | 05694310963756 | 20 mm Circular | 50215H51B0D | Bilayer wound management medical device product made from fish skin and silicone Bilayer wound management medical device product made from fish skin and silicone. Kerecis® Omega3 MariGen® Shield is indicated for the management of wounds including: Partial and full-thickness wounds, Pressure ulcers, Venous ulcers, Chronic vascular ulcers, Diabetic ulcers, Trauma wounds (abrasions, lacerations, partial-thickness burns, skin tears), Surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and Draining wounds. https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen-shield/ | Kerecis® Omega3 MariGen® Shield | KERECIS HF. |
23 | 05694310962438 | 7x10 cm | 50200S03B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
24 | 05694310962414 | 3x7 cm | 50200S02B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
25 | 05694310962391 | 3x3.5 cm | 50200S01B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen | Kerecis® Omega3 MariGen | KERECIS HF. |
26 | 05694310962230 | Expanse 8x10 cm | 50200N13B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
27 | 05694310962216 | Expanse 7x8 cm | 50200N11B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
28 | 05694310961653 | Micro 38 sq cm | 50200P04D0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
29 | 05694310961615 | Micro 19 sq cm | 50200P02D0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
30 | 05694310961592 | Micro 8 sq cm | 50200P01B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
31 | 05694310961578 | Micro 4 sq cm | 50200P00B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
32 | 05694310961554 | Micro 38 sq cm | 50205P04D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
33 | 05694310961530 | Micro 19 sq cm | 50205P02D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose™ is indicated for t Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose™ is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds. IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose™ | KERECIS HF. |
34 | 05694310961493 | Micro 19 sq cm | 50205P02D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
35 | 05694310961158 | 7x20 cm Meshed 2:1 | 50205N21D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
36 | 05694310961134 | 7x10 cm Meshed 2:1 | 50205N03D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
37 | 05694310961110 | 7x20 Meshed Burn | 50202N21D0D | Acellular fish skin for topical and surgical wounds.INTENDED USEKerecis® Burn is Acellular fish skin for topical and surgical wounds.INTENDED USEKerecis® Burn is indicated for the management of wounds including: - Partial and full-thickness wounds, - Trauma wounds (abrasions, lacerations, second-degree burns, skin tears).Mesh ratio 2:1Double Pouchedhttps://www.kerecis.com/wp-content/uploads/2020/10/A5-KM-19-0146-IFU-Kerecis-Burn-US.pdf | Kerecis® Omega3 BURN | KERECIS HF. |
38 | 05694310961097 | 7x10 cm Meshed | 50202N03D0D | Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indica Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indicated for the management of wounds including: Partial and full thickness wounds, Trauma wounds including second degree burns, Surgical wounds including donor sites/ grafts.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-graftguide/ | Kerecis® Omega3 GraftGuide™ | KERECIS HF. |
39 | 05694310961059 | 300 sq cm Meshed 2:1 | 50205N23D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
40 | 05694310961035 | 250 sq cm Meshed 2:1 | 50205N24D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
41 | 05694310961011 | 300 sq cm Meshed | 50202N23D0D | Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indica Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indicated for the management of wounds including: Partial and full thickness wounds, Trauma wounds including second degree burns, Surgical wounds including donor sites/ grafts.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-graftguide/ | Kerecis® Omega3 GraftGuide™ | KERECIS HF. |
42 | 05694310960991 | 250 sq cm Meshed | 50202N24D0D | Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indica Fish-Skin Graft for Burn Wound Management. Kerecis® Omega3 GraftGuide™ is indicated for the management of wounds including: Partial and full thickness wounds, Trauma wounds including second degree burns, Surgical wounds including donor sites/ grafts.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-graftguide/ | Kerecis® Omega3 GraftGuide™ | KERECIS HF. |
43 | 05694310960977 | 7x7 Particularized Wound | 50200P04D0D | "Acellular fish skin for topical and surgical wounds.INTENDED USE Kerecis® Omega "Acellular fish skin for topical and surgical wounds.INTENDED USE Kerecis® Omega 3 Wound is indicated for the management of wounds including:•Partial and full-thickness wounds •Pressure ulcers •Venous ulcers •Chronic vascular ulcers •Diabetic ulcers •Trauma wounds (abrasions, lacerations, second-degree burns, skin tears) •Surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) •Draining WoundsParticularized, double pouchhttps://www.kerecis.com/wp-content/uploads/2020/11/Instructions-for-Use-IFU.pdf" | Kerecis® Omega3 Wound | KERECIS HF. |
44 | 05694310960953 | 3x7 Fragmented Wound | 50200P02D0D | "Acellular fish skin for topical and surgical wounds.INTENDED USE Kerecis® Omega "Acellular fish skin for topical and surgical wounds.INTENDED USE Kerecis® Omega 3 Wound is indicated for the management of wounds including:•Partial and full-thickness wounds •Pressure ulcers •Venous ulcers •Chronic vascular ulcers •Diabetic ulcers •Trauma wounds (abrasions, lacerations, second-degree burns, skin tears) •Surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) •Draining WoundsParticularized, double pouchhttps://www.kerecis.com/wp-content/uploads/2020/11/Instructions-for-Use-IFU.pdf" | Kerecis® Omega3 Wound | KERECIS HF. |
45 | 05694310960939 | 3x3.5 Particularized Wound | 50200P01D0D | Acellular fish skin for topical and surgical wounds."Acellular fish skin for top Acellular fish skin for topical and surgical wounds."Acellular fish skin for topical and surgical wounds.INTENDED USE Kerecis® Omega 3 Wound is indicated for the management of wounds including:•Partial and full-thickness wounds •Pressure ulcers •Venous ulcers •Chronic vascular ulcers •Diabetic ulcers •Trauma wounds (abrasions, lacerations, second-degree burns, skin tears) •Surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) •Draining WoundsParticularized, double pouchhttps://www.kerecis.com/wp-content/uploads/2020/11/Instructions-for-Use-IFU.pdf" | Kerecis® Omega3 Wound | KERECIS HF. |
46 | 05694310960892 | 5x7 cm | 50200S05B0D | Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for th Fish-skin graft for wound management. Kerecis Omega3 MariGen is indicated for the management of wounds including: Partial and full-thickness wounds, pressure ulcers, venous ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor sites/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-marigen/ | Kerecis® Omega3 MariGen | KERECIS HF. |
47 | 05694310960786 | 300 sq cm | 50205S23D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
48 | 05694310960762 | 250 sq cm | 50205S24D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
49 | 05694310960748 | 10x25 cm | 50205S22D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |
50 | 05694310960724 | 7x20 cm | 50205S21D0D | Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for th Fish-Skin Graft for Surgical Use. Kerecis® Omega3 SurgiClose is indicated for the management of wounds including: Partial and full thickness wounds, pressure ulcers, chronic vascular ulcers, diabetic ulcers, trauma wounds (abrasions, lacerations, second-degree burns, skin tears), surgical wounds (donor site/grafts, post-Mohs surgery, post-laser surgery, podiatric, wound dehiscence) and draining wounds.IFU: https://www.kerecis.com/ifus/ifu-kerecis-omega3-surgiclose/ | Kerecis® Omega3 SurgiClose | KERECIS HF. |