No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | D765RTM304010 | RTM3040-1 | Resorbable Bovine Collagen Barrier Membrane, 30mm x 40mm, Sterile, Contents: 1 Membrane | NPL | Barrier, Animal Source, Intraoral | 2 | CYTOPLAST RTM COLLAGEN | |
2 | D765RTM30401 | RTM3040 | Resorbable Bovine Collagen Barrier Membrane, 30mm x 40mm, Sterile, Contents: 2 Membranes | NPL | Barrier, Animal Source, Intraoral | CYTOPLAST RTM COLLAGEN | ||
3 | D765RTM203010 | RTM2030-1 | Resorbable Bovine Collagen Barrier Membrane, 20mm x 30mm, Sterile, Contents: 1 Membrane | NPL | Barrier, Animal Source, Intraoral | 2 | CYTOPLAST RTM COLLAGEN | |
4 | D765RTM20301 | RTM2030 | Resorbable Bovine Collagen Barrier Membrane, 20mm x 30mm, Sterile, Contents: 2 Membranes | NPL | Barrier, Animal Source, Intraoral | CYTOPLAST RTM COLLAGEN | ||
5 | D765RTM152010 | RTM1520-1 | Resorbable Bovine Collagen Barrier Membrane, 15mm x 20mm, Sterile, Contents: 1 Membrane | NPL | Barrier, Animal Source, Intraoral | 2 | CYTOPLAST RTM COLLAGEN | |
6 | D765RTM15201 | RTM1520 | Resorbable Bovine Collagen Barrier Membrane, 15mm x 20mm, Sterile, Contents: 2 Membranes | NPL | Barrier, Animal Source, Intraoral | CYTOPLAST RTM COLLAGEN | ||
7 | D765TI250XLN20 | Ti250XL-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
8 | D765TI250XLN10 | Ti250XL-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
9 | D765TI250XLKN20 | Ti250XLK-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced,30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
10 | D765TI250XLKN10 | Ti250XLK-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
11 | D765TI250PTCN20 | Ti250PTC-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 38 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
12 | D765TI250PTCN10 | Ti250PTC-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 38 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
13 | D765TI250PSTN20 | Ti250PST-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 25 mm 36 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
14 | D765TI250PSTN10 | Ti250PST-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 25 mm x 36 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
15 | D765TI250PSN20 | Ti250PS-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 20 mm x 25 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
16 | D765TI250PSN10 | Ti250PS-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 20 mm x 25 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
17 | D765TI250PPN20 | Ti250PP-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 13 mm x 18 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
18 | D765TI250PPN10 | Ti250PP-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 13 mm x 18 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
19 | D765TI250PLTN20 | Ti250PLT-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 41 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
20 | D765TI250PLTN10 | Ti250PLT-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 41 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
21 | D765TI250PLN20 | Ti250PL-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 25 mm x 30 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
22 | D765TI250PLN10 | Ti250PL-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 25 mm x 30 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
23 | D765TI250PDN20 | Ti250PD-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 38 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
24 | D765TI250PDN10 | Ti250PD-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 38 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
25 | D765TI250K2N20 | Ti250K2-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 40 mm x 50 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
26 | D765TI250K2N10 | Ti250K2-N-1 | Non-resorbable Textured PTFE Barrier Membranes, Titanium- Reinforced, 40 mm x 50 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
27 | D765TI250BLN20 | Ti250BL-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 17 mm x 25 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
28 | D765TI250BLN10 | Ti250BL-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 17 mm x 25 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
29 | D765TI250BLLN20 | Ti250BLL-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 17 mm x 30 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
30 | D765TI250BLLN10 | Ti250BLL-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 17 mm x 30 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
31 | D765TI250ATCN10 | Ti250ATC-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 24 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
32 | D765TI250ASN20 | Ti250AS-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 14 mm x 24 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
33 | D765TI250ASN10 | Ti250AS-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 14 mm x 24 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
34 | D765TI250APN20 | Ti250AP-N-2 | Nonresorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 13 mm x 19 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
35 | D765TI250APN10 | Ti250AP-N-1 | Nonresorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 13 mm x 19 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
36 | D765TI250ANLN20 | TI250ANL-N-2 | Nonresorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 12 mm x 24 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
37 | D765TI250ANLN10 | Ti250ANL-N-1 | Nonresorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 12 mm x 24 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
38 | D765TI250ANL30N20 | Ti250ANL30-N-2 | Non-Resorbable Textured PTFE Barrier Membrane, 12 mm x 30 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
39 | D765TI250ANL30N10 | Ti250ANL30-N-1 | Non-Resorbable Textured PTFE Barrier Membrane, 12 mm x 30 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
40 | D765TI150XLN20 | Ti150XL-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
41 | D765TI150XLN10 | Ti150XL-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
42 | D765TI150XLKN20 | Ti150XLK-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
43 | D765TI150XLKN10 | Ti150XLK-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 40 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
44 | D765TI150PTCN20 | Ti150PTC-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 38 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
45 | D765TI150PTCN10 | Ti150PTC-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 38 mm x 38 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
46 | D765TI150PSTN20 | Ti150PST-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 25 mm x 36 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
47 | D765TI150PSTN10 | Ti150PST-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 25 mm x 36 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
48 | D765TI150PSN20 | Ti150PS-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 20 mm x 25 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
49 | D765TI150PSN10 | Ti150PS-N-1 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 20 mm x 25 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes | |
50 | D765TI150PLTN20 | Ti150PLT-N-2 | Non-resorbable Textured PTFE Barrier Membrane, Titanium-Reinforced, 30 mm x 41 mm | NPK | Barrier, Synthetic, Intraoral | 2 | Cytoplast™ Titanium-Reinforced PTFE Membranes |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 08809186549516 | CB-0110-050 | OCS-B Collagen® is a combination of purified cancellous bone mineral granules (O OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | OCS-B Collagen | NIBEC CO., LTD. | |
2 | 08809186549509 | CB-0110-025 | OCS-B Collagen® is a combination of purified cancellous bone mineral granules (O OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | OCS-B Collagen | NIBEC CO., LTD. | |
3 | 08809186549493 | CB-0110-005 | OCS-B Collagen® is a combination of purified cancellous bone mineral granules (O OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | OCS-B Collagen | NIBEC CO., LTD. | |
4 | 08809186549455 | RSP2-L | Regenomer® is a sponge-like absorbable and porous collagen designed to be used a Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Regenomer | NIBEC CO., LTD. | |
5 | 08809186549448 | RSP1-S | Regenomer® is a sponge-like absorbable and porous collagen designed to be used a Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Regenomer | NIBEC CO., LTD. | |
6 | 08809186549431 | RSB2-L | Regenomer® is a sponge-like absorbable and porous collagen designed to be used a Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Regenomer | NIBEC CO., LTD. | |
7 | 08809186549424 | RSB1-S | Regenomer® is a sponge-like absorbable and porous collagen designed to be used a Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Regenomer® is manufactured in three types, Regenomer® Syringe (sheet shape in syringe and blister), Regenomer® Plug (bullet shape in blister), and Regenomer® Block (block shape in blister). Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Regenomer | NIBEC CO., LTD. | |
8 | 08809186549349 | CB-0110-010 | OCS-B Collagen® is a combination of purified cancellous bone mineral granules (O OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | OCS-B Collagen | NIBEC CO., LTD. | |
9 | 08809186549332 | CB-0110-050S | OCS-B Collagen® is a combination of purified cancellous bone mineral granules (O OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | OCS-B Collagen | NIBEC CO., LTD. | |
10 | 08809186549325 | CB-0110-025S | OCS-B Collagen® is a combination of purified cancellous bone mineral granules (O OCS-B Collagen® is a combination of purified cancellous bone mineral granules (OCS-B®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | OCS-B Collagen | NIBEC CO., LTD. | |
11 | 08809186549127 | L1-1020-050 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
12 | 08809186549110 | L1-1020-025 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
13 | 08809186549080 | L1-0210-050 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
14 | 08809186549073 | L1-0210-025 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
15 | 08809186548908 | S1-1020-200 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
16 | 08809186548892 | S1-1020-100 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
17 | 08809186548885 | S1-1020-050 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
18 | 08809186548878 | S1-1020-025 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
19 | 08809186548861 | S1-0210-200 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
20 | 08809186548854 | S1-0210-100 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
21 | 08809186548847 | S1-0210-050 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
22 | 08809186548830 | S1-0210-025 | Straumann Xenograft bone grafting material is a sterile, porous bone mineral mat Straumann Xenograft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. Straumann Xenograft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Straumann Xenograft is effective for the regeneration of new bone around the grafted bone. The Straumann Xenograft has good osteoconductivity to enhance new bone formation. | Straumann Xenograft | NIBEC CO., LTD. | |
23 | 08809186542067 | RSB2-L | Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed t Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types, Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Straumann Regenomer | NIBEC CO., LTD. | |
24 | 08809186542050 | RSB1-S | Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed t Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types,Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Straumann Regenomer | NIBEC CO., LTD. | |
25 | 08809186542043 | RSP2-L | Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed t Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types, Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Straumann Regenomer | NIBEC CO., LTD. | |
26 | 08809186542036 | RSP1-S | Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed t Straumann® Regenomer® is a sponge-like absorbable and porous collagen designed to be used as bone filling augmentation material. The device is manufactured from purified type I collagen derived from porcine skin sources in South Korea. The porcine skin is certified by veterinarian and is obtained by a standardized controlled manufacturing process. Straumann® Regenomer® is manufactured in three types, Straumann® Regenomer® Syringe (sheet shape in syringe and blister), Straumann® Regenomer® Plug (bullet shape in blister), and Straumann® Regenomer® Block (block shape in blister). Straumann® Regenomer® are supplied sterile, non-pyrogenic, and for single use only. | Straumann Regenomer | NIBEC CO., LTD. | |
27 | 08809186542029 | I1-1020-200 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
28 | 08809186542012 | I1-1020-100 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
29 | 08809186542005 | I1-1020-050 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
30 | 08809186541992 | I1-1020-025 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
31 | 08809186541985 | I1-0210-200 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
32 | 08809186541978 | I1-0210-100 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
33 | 08809186541961 | I1-0210-050 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
34 | 08809186541954 | I1-0210-025 | The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral m The Neodent XenoGraft bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The Neodent XenoGraft contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of Neodent XenoGraft is effective for the regeneration of new bone around the grafted bone. The Neodent XenoGraft has good osteoconductivity to enhance new bone formation. The Neodent XenoGraft are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | Neodent XenoGraft | NIBEC CO., LTD. | |
35 | 08809186541800 | NI-0110-050S | Straumann XenoFlex® is a combination of purified cancellous bone mineral granule Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Straumann XenoFlex | NIBEC CO., LTD. | |
36 | 08809186541794 | NI-0110-025S | Straumann XenoFlex® is a combination of purified cancellous bone mineral granule Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Straumann XenoFlex | NIBEC CO., LTD. | |
37 | 08809186541787 | NI-0110-050 | Straumann XenoFlex® is a combination of purified cancellous bone mineral granule Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Straumann XenoFlex | NIBEC CO., LTD. | |
38 | 08809186541770 | NI-0110-025 | Straumann XenoFlex® is a combination of purified cancellous bone mineral granule Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Straumann XenoFlex | NIBEC CO., LTD. | |
39 | 08809186541763 | NI-0110-010 | Straumann XenoFlex® is a combination of purified cancellous bone mineral granule Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Straumann XenoFlex | NIBEC CO., LTD. | |
40 | 08809186541756 | NI-0110-005 | Straumann XenoFlex® is a combination of purified cancellous bone mineral granule Straumann XenoFlex® is a combination of purified cancellous bone mineral granules (Straumann Xenograft®) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Straumann XenoFlex | NIBEC CO., LTD. | |
41 | 08809186541718 | S1-0210-025 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
42 | 08809186541701 | S1-0210-050 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
43 | 08809186541695 | S1-0210-100 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
44 | 08809186541688 | S1-0210-200 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
45 | 08809186541671 | S1-1020-025 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
46 | 08809186541664 | S1-1020-050 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
47 | 08809186541657 | S1-1020-100 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
48 | 08809186541640 | S1-1020-200 | The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, The OCS-B OsteoConductive Substitute-Bovine bone grafting material is a sterile, porous bone mineral matrix produced by the removal of the organic compounds from bovine bone. The OCS-B contains pure hydroxyapatite derived from bovine bone using a validated the manufacturing process. The large surface area of OCS-B is effective for the regeneration of new bone around the grafted bone. The OCS-B has good osteoconductivity to enhance new bone formation. The OCS-Bs are supplied as cancellous (spongiosa) or cortical granules in single-use containers. | OCS-B | NIBEC CO., LTD. | |
49 | 08809186540841 | N1420 | Creos Xenogain Collagen is a combination of purified cancellous bone mineral gra Creos Xenogain Collagen is a combination of purified cancellous bone mineral granules (Creos Xenogain) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Creos Xenogain Collagen | NIBEC CO., LTD. | |
50 | 08809186540834 | N1410 | Creos Xenogain Collagen is a combination of purified cancellous bone mineral gra Creos Xenogain Collagen is a combination of purified cancellous bone mineral granules (Creos Xenogain) and 10% collagen in a block form in a blister and cylindrical form in a syringe and blister. It is sterilized by γ- irradiation. | Creos Xenogain Collagen | NIBEC CO., LTD. |