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.
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.
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.
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.
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.
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.
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.
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.
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)
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)
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)
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porou
InRoad® Dental Synthetic Bone Graft (SBG) is a synthetic, semi-dense multi-porous bioceramic for bone regeneration. It is comprised of 90% ± 5% hydroxyapatite (HA) and 10% ± 5% Beta-Tricalcium Phosphate. The granules are provided sterile (gamma irradiated) in a capped vial packaged in a lid sealed tray. InRoad® Dental SBG granules are designed to resemble trabecular bone structure. The granule structure consists of interconnected primary open pores, secondary channel-like structure, and tertiary small holes on the surface in a biocompatible and osteoconductive biomaterial. The multi-porous structure of InRoad® Dental SBG makes it possible for the bone cells to migrate into the matrices and for new bone to grow. InRoad® Dental SBG is available in granule form in sizes of 0.3 – 1.0 mm (Small) and 0.8 – 1.8 mm (Large).
#ORAMEM SUS 30x40OraMem Sustained absorbable collagen membrane is an absorbable
#ORAMEM SUS 30x40OraMem Sustained absorbable collagen membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.OraMem Sustained absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achillies) tendon. Bovine tendon is known to be one of the purest sources of Type I collagen that can be readily obtained and processed in commercial amounts. The OraMem Sustained membrane is completely absorbable, eliminating the need for the second surgical procedure required to remove a non-resorbable membrane. The collagen is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
#ORAMEM SUS 20x30OraMem Sustained absorbable collagen membrane is an absorbable
#ORAMEM SUS 20x30OraMem Sustained absorbable collagen membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.OraMem Sustained absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achillies) tendon. Bovine tendon is known to be one of the purest sources of Type I collagen that can be readily obtained and processed in commercial amounts. The OraMem Sustained membrane is completely absorbable, eliminating the need for the second surgical procedure required to remove a non-resorbable membrane. The collagen is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
#ORAMEM SUS 15x20OraMem Sustained absorbable collagen membrane is an absorbable
#ORAMEM SUS 15x20OraMem Sustained absorbable collagen membrane is an absorbable, implantable material that is indicated for guided tissue regeneration procedures in periodontal defects to enhance regeneration of the periodontal apparatus.OraMem Sustained absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achillies) tendon. Bovine tendon is known to be one of the purest sources of Type I collagen that can be readily obtained and processed in commercial amounts. The OraMem Sustained membrane is completely absorbable, eliminating the need for the second surgical procedure required to remove a non-resorbable membrane. The collagen is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
ORAMEM 30x40OraMem absorbable collagen membrane is a white, compressed, non-fria
ORAMEM 30x40OraMem absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon. The OraMem membrane is completely absorbable, eliminating the need for the second surgical procedure often required to remove a non-resorbabble membrane. The collage is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
ORAMEM 20x30OraMem absorbable collagen membrane is a white, compressed, non-fria
ORAMEM 20x30OraMem absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon. The OraMem membrane is completely absorbable, eliminating the need for the second surgical procedure often required to remove a non-resorbabble membrane. The collage is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
ORAMEM 15x20OraMem absorbable collagen membrane is a white, compressed, non-fria
ORAMEM 15x20OraMem absorbable collagen membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon. The OraMem membrane is completely absorbable, eliminating the need for the second surgical procedure often required to remove a non-resorbabble membrane. The collage is currently used for general and dental surgery as absorbable hemostatic agents and absorbable wound dressings.
BIOMEND EXTEND 30MM X 40MM (0142) BioMend Extend Absorbable Collagen Membrane is
BIOMEND EXTEND 30MM X 40MM (0142) BioMend Extend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend Extend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND 30MM X 40MM (0107)BioMend Absorbable Collagen Membrane is an absorbab
BIOMEND 30MM X 40MM (0107)BioMend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus.The BioMend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND EXTEND 20MM X 30MM (0141) BioMend Extend Absorbable Collagen Membrane is
BIOMEND EXTEND 20MM X 30MM (0141) BioMend Extend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend Extend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND 20MM X 30MM (0105) BioMend Absorbable Collagen Membrane is an absorbable
BIOMEND 20MM X 30MM (0105) BioMend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND EXTEND 15MM X 20MM (0140) BioMend Extend Absorbable Collagen Membrane is
BIOMEND EXTEND 15MM X 20MM (0140) BioMend Extend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus. The BioMend Extend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
BIOMEND 15 MM X 20 MM(0103)BioMend Absorbable Collagen Membrane is an absorbabl
BIOMEND 15 MM X 20 MM(0103)BioMend Absorbable Collagen Membrane is an absorbable, implantable material that is indicated for guided tissue generation procedures in periodontal defects to enhance regeneration of periodontal apparatus.The BioMend membrane is a white, compressed, non-friable matrix fabricated from collagen derived from bovine deep flexor (Achilles) tendon.
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.
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.
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.
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.
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.
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.