Other products from "UNICARE BIOMEDICAL INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 D767C0245010 M4-500 C02-4501 Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. JEY Plate, Bone 2 Cytoflex Mesh
2 D767C0244010 M4-400 C02-4401 Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. JEY Plate, Bone 2 Cytoflex Mesh
3 D767C0243010 M4-300 C02-4301 Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. JEY Plate, Bone 2 Cytoflex Mesh
4 D767C0242010 M4-200 C02-4201 Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. JEY Plate, Bone 2 Cytoflex Mesh
5 D767C0241010 M4-100 C02-4101 Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profil Cytoflex® Mesh is made of pure implantable Titanium with a precision mesh profile. This product is designed for use to ensure three-dimensional reconstruction of alveolar bone defects and to facilitate bone augmentation through adequate fixation of the augmentation material. The thin, supple mesh conforms easily to tissue contours, and yet presents sufficient stiffness to maintain space over the bony defect. JEY Plate, Bone 2 Cytoflex Mesh
6 D767B0103081 C-003 B01-0308 BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic BenaCel
7 D767B0102121 C-002 B01-0212 BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic BenaCel
8 D767B0105101 C-005 B01-0510 BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic BenaCel
9 D767B0104081 C-004 B01-0408 BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation. BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic U BenaCel
10 D767B0101081 C-001 B01-0108 BenaCel® dental dressing is made of biocompatible oxidized cellulose and contain BenaCel® dental dressing is made of biocompatible oxidized cellulose and contains no chemical additives. BenaCel® dental dressing adheres to moist oral mucosa and forms a temporary barrier protecting the wound from further irritation and pain. When placed in the extraction socket, BenaCel® dental dressing forms a gelatinous scaffold in the blood extrude, facilitating the development of a stable blood clot to prevent dry socket formation.BenaCel® dental dressing is designed for use in the extraction site and the management of bleeding and alveolar osteitis (dry socket). It may also be used as a wound dressing for the temporary management of oral surgical wounds, such as operative, postoperative, donor sites and traumatic injuries. MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic BenaCel
11 D767C0302010 20x25mm C03-0201 Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytofl Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex® Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex® Resorb barriers are resorbable and do not require a second retrieval procedure. NPK Barrier, Synthetic, Intraoral 2 Cytoflex Resorb
12 D767C0301010 30x40mm C03-0101 Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytofl Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex® Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex® Resorb barriers are resorbable and do not require a second retrieval procedure. NPK Barrier, Synthetic, Intraoral 2 Cytoflex Resorb
13 D767C0303010 12x24mm C03-0301 Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytofl Cytoflex® Resorb is a synthetic, microporous resorbable barrier membrane. Cytoflex® Resorb membranes are designed to enhance the adhesion of host cells, and at the same time provide a favorable environment for neo-vascularization and repopulation of bone cells to regenerate osseous tissue. The flexible barrier membranes are easily adaptable to tissue contours, yet offer sufficient duration to protect the bony defect from the intrusion of bacteria and soft tissue. Composed of synthetic polylactide and polyglycolide copolymers, Cytoflex® Resorb barriers are resorbable and do not require a second retrieval procedure. NPK Barrier, Synthetic, Intraoral 2 Cytoflex Resorb
14 D767U0302051 200-600um 1.0g U03-0205 Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. LYC Bone Grafting Material, Synthetic Unigraft
15 D767U0301051 200-600um 0.4g U03-0105 Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. LYC Bone Grafting Material, Synthetic Unigraft
16 D767U0102051 200-400um 1.0g U01-0205 Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. LYC Bone Grafting Material, Synthetic Unigraft
17 D767U0101051 200-400um 0.4g U01-0105 Unigraft is made of synthetic bioactive glass material. The product is convenien Unigraft is made of synthetic bioactive glass material. The product is conveniently packaged in a sterile vial and stored within a hermetically sealed foil pouch to ensure product sterility prior to implantation. Unigraft offers an osteogenic framework for new bone growth and bolsters a higher level of osteoblastic activity to enhance bone regeneration. FDA has cleared this product for use in treating periodontal defects, extractions sites, sinus elevation, apicoectomy and root resection, cranial and facial augmentation and augmentation of the alveolar ridges. LYC Bone Grafting Material, Synthetic Unigraft
18 D767C0101010 TEF-002 C01-0101 Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. NPK Barrier, Synthetic, Intraoral 2 Cytoflex Smooth Tef-Guard
19 D767C0402010 TEX-200 C04-0201 Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE), the textured version of Cytoflex® Tef-Guard® has superficial macro texture overlapping the micro pore texture on both surfaces. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. The macro texture provides additional grips for flap attachment. NPK Barrier, Synthetic, Intraoral Cytoflex Textured Tef-Guard
20 D767C0401010 TEX-100 C04-0101 Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barr Cytoflex® Tef-Guard® is a non-resorbable membrane for use as a space-making barrier in guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE) thin film, Cytoflex® Tef-Guard® has a surface texture and porosity suitable for adhesion of host cells to the material while blocking passage and integration of bacteria within the interstices of the material. The supple membrane conforms easily to tissue contours, and yet offers sufficient stiffness to maintain a space over the bony defect. The micro porous surface is designed to improve flap attachment but prevent tissue and bacteria ingrowth. Cytoflex® Tef-Guard® is for use as a barrier membrane for guided tissue regeneration procedures. Composed of a proprietary micro-porous polytetrafluoroethylene (ePTFE), the textured version of Cytoflex® Tef-Guard® has superficial macro texture overlapping the micro pore texture on both surfaces. The cellular level micro texture is invisible to the naked eye, but can be seen at high magnifications. The macro texture provides additional grips for flap attachment. NPK Barrier, Synthetic, Intraoral 2 Cytoflex Textured Tef-Guard
Other products with the same Product Code "NPK"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M224TCK20139 1 TCK-2013 Tacks (4 x) Inion GTR™ INION OY
2 M224TCK20119 1 TCK-2011 Tacks, drill bit and tack appl. Inion GTR™ INION OY
3 M224TCK20029 1 TCK-2002 Tacks and drill bit Inion GTR™ INION OY
4 M224MBR20009 1 MBR-2000 Membrane 30x40 mm Inion GTR™ INION OY
5 M224INS90529 0 INS-9052 Re-usable tack applicator Inion GTR instrument INION OY
6 M224INS905210 1 INS-9052 Re-usable tack applicator Inion GTR instrument INION OY
7 07630031726834 1 070.102 Straumann® MembraGel , Applicator STRAUMANN MEMBRAGEL INSTITUT STRAUMANN AG
8 07630031700148 1 070.101 Straumann® MembraGel® 0.8 ml STRAUMANN MEMBRAGEL INSTITUT STRAUMANN AG
9 07613252204480 81073 81073 MEDPOR¿ CONTAIN? CAN Implant with Protective Spacer MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
10 07613252204466 81072 81072 MEDPOR¿ CONTAIN? CAN Implant with Protective Spacer MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
11 07613252204459 81071 81071 MEDPOR¿ CONTAIN? CAN Implant with Protective Spacer MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
12 07613252084495 81068 81068 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
13 07613252084488 81067 81067 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
14 07613252084471 81066 81066 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
15 07613252084464 81065 81065 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
16 07613252084457 81064 81064 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
17 07613252084440 81063 81063 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
18 07613252084433 81062 81062 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
19 07613252084426 81061 81061 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
20 07613252084419 81060 81060 MEDPOR¿ CONTAIN? Implant Sheet MEDPOR CONTAIN STRYKER LEIBINGER GMBH & CO. KG
21 07332747193497 N1615TI-A13-1 N1615TI-A13-1 creos syntoprotect Ti-150 No13 creos™ syntoprotect NOBEL BIOCARE AB
22 07332747193480 N1615TI-A12-1 N1615TI-A12-1 creos syntoprotect Ti-150 No12 creos™ syntoprotect NOBEL BIOCARE AB
23 07332747193473 N1615TI-A11-1 N1615TI-A11-1 creos syntoprotect Ti-150 No11 creos™ syntoprotect NOBEL BIOCARE AB
24 07332747193466 N1615TI-A10-1 N1615TI-A10-1 creos syntoprotect Ti-150 No10 creos™ syntoprotect NOBEL BIOCARE AB
25 07332747193459 N1615TI-A09-1 N1615TI-A09-1 creos syntoprotect Ti-150 No9 creos™ syntoprotect NOBEL BIOCARE AB
26 07332747193442 N1615TI-A08-1 N1615TI-A08-1 creos syntoprotect Ti-150 No8 creos™ syntoprotect NOBEL BIOCARE AB
27 07332747193435 N1615TI-A07-1 N1615TI-A07-1 creos syntoprotect Ti-150 No7 creos™ syntoprotect NOBEL BIOCARE AB
28 07332747193411 N1615TI-A06-1 N1615TI-A06-1 creos syntoprotect Ti-150 No6 creos™ syntoprotect NOBEL BIOCARE AB
29 07332747193404 N1615TI-A05-1 N1615TI-A05-1 creos syntoprotect Ti-150 No5 creos™ syntoprotect NOBEL BIOCARE AB
30 07332747193398 N1615TI-A04-1 N1615TI-A04-1 creos syntoprotect Ti-150 No4 creos™ syntoprotect NOBEL BIOCARE AB
31 07332747193381 N1615TI-A03-1 N1615TI-A03-1 creos syntoprotect Ti-150 No3 creos™ syntoprotect NOBEL BIOCARE AB
32 07332747193374 N1615TI-A02-1 N1615TI-A02-1 creos syntoprotect Ti-150 No2 creos™ syntoprotect NOBEL BIOCARE AB
33 07332747193367 N1615TI-A01-1 N1615TI-A01-1 creos syntoprotect Ti-150 No1 creos™ syntoprotect NOBEL BIOCARE AB
34 07332747193350 N1625TI-A13-1 N1625TI-A13-1 creos syntoprotect Ti-250 No13 creos™ syntoprotect NOBEL BIOCARE AB
35 07332747193343 N1625TI-A12-1 N1625TI-A12-1 creos syntoprotect Ti-250 No12 creos™ syntoprotect NOBEL BIOCARE AB
36 07332747193336 N1625TI-A11-1 N1625TI-A11-1 creos syntoprotect Ti-250 No11 creos™ syntoprotect NOBEL BIOCARE AB
37 07332747193329 N1625TI-A10-1 N1625TI-A10-1 creos syntoprotect Ti-250 No10 creos™ syntoprotect NOBEL BIOCARE AB
38 07332747193312 N1625TI-A09-1 N1625TI-A09-1 creos syntoprotect Ti-250 No9 creos™ syntoprotect NOBEL BIOCARE AB
39 07332747193305 N1625TI-A08-1 N1625TI-A08-1 creos syntoprotect Ti-250 No8 creos™ syntoprotect NOBEL BIOCARE AB
40 07332747193299 N1625TI-A07-1 N1625TI-A07-1 creos syntoprotect Ti-250 No7 creos™ syntoprotect NOBEL BIOCARE AB
41 07332747193282 N1625TI-A06-1 N1625TI-A06-1 creos syntoprotect Ti-250 No6 creos™ syntoprotect NOBEL BIOCARE AB
42 07332747193275 N1625TI-A05-1 N1625TI-A05-1 creos syntoprotect Ti-250 No5 creos™ syntoprotect NOBEL BIOCARE AB
43 07332747193251 N1625TI-A04-1 N1625TI-A04-1 creos syntoprotect Ti-250 No4 creos™ syntoprotect NOBEL BIOCARE AB
44 07332747193244 N1625TI-A03-1 N1625TI-A03-1 creos syntoprotect Ti-250 No3 creos™ syntoprotect NOBEL BIOCARE AB
45 07332747193237 N1625TI-A02-1 N1625TI-A02-1 creos syntoprotect Ti-250 No2 creos™ syntoprotect NOBEL BIOCARE AB
46 07332747193220 N1625TI-A01-1 N1625TI-A01-1 creos syntoprotect Ti-250 No1 creos™ syntoprotect NOBEL BIOCARE AB
47 05060440334931 64019 64019 NeoGen® PTFE Membrane, Non-Reinforced 18 x 12 mm Neoss Implant System NEOSS AB
48 05060440334924 64015 64015 NeoGen® PTFE Membrane, Ti-Reinforced - XL Neoss Implant System NEOSS AB
49 05060440331626 64021 64021 NeoGen® PTFE Membrane, Non-Reinforced 34 x 25 mm Neoss Implant System NEOSS AB
50 05060440331619 64020 64020 NeoGen PTFE Membrane, Non-Reinforced 29 x 14 mm Neoss Implant System NEOSS AB