No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00889024597624 | 110043606 | 110043606 | MBH,JWH,OIY | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | Persona® | |
2 | 00889024597549 | 110043598 | 110043598 | OIY,JWH,MBH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER | 2 | Persona® | |
3 | 00889024597518 | 110043595 | 110043595 | OIY,MBH,JWH | Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Persona® | |
4 | 00889024597471 | 110043591 | 110043591 | MBH,JWH,OIY | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | Persona® | |
5 | 00889024481916 | 01.03916.445 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
6 | 00889024481893 | 01.03916.435 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
7 | 00889024481862 | 01.03916.045 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
8 | 00889024594531 | 02.60000.008 | HWT | Template | 1 | NCB® | ||
9 | 00889024592131 | 01.04215.183 | 01.04215.183 | PHX,HSD,KWT,KWS | shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, HEMI-, HUMERAL, shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED | 2 | Anatomical Shoulder™ | |
10 | 00889024592032 | 01.00551.213 | 01.00551.213 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
11 | 00889024592018 | 01.00551.312 | 01.00551.312 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
12 | 00889024591936 | 01.00551.310 | 01.00551.310 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
13 | 00889024590663 | 2852 | 2852 | KWL,JDI,LZO,KWY | Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/ Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Alloclassic® Zweymüller® | |
14 | 00889024590656 | 01.00121.100 | 01.00121.100 | JDI,KWY,LZO,KWL | Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, hemi Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, hemi-, femoral, metal | 2 | Alloclassic® Zweymüller® | |
15 | 00889024590465 | 2848 | 2848 | KWL,KWY,JDI,LZO | Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, hemi-, femoral, metal/po Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented | 2 | Alloclassic® Zweymüller® | |
16 | 00889024577909 | 110040870 | 110040870 | MBH,OIY,JWH | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER | 2 | Persona® | |
17 | 00889024577862 | 110040866 | 110040866 | JWH,MBH,OIY | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | Persona® | |
18 | 00889024591837 | 01.00551.208 | 01.00551.208 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
19 | 00889024591820 | 01.00551.110 | 01.00551.110 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
20 | 00889024577589 | 110040839 | 110040839 | MBH,JWH,OIY | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive | 2 | Persona® | |
21 | 00889024509818 | 110038119 | 110038119 | HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES | 2 | Affixus® Natural Nail® | |
22 | 00889024506664 | 110035675 | 110035675 | HSB | ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES | 2 | Affixus® Natural Nail® | |
23 | 00889024591639 | 01.00551.204 | 01.00551.204 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
24 | 00889024591615 | 01.00551.401 | 01.00551.401 | JDI,KWL,KWY,KWZ,LWJ,LZO | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | Fitmore® | |
25 | 00889024590939 | 01.06010.002 | 01.06010.002 | LWJ,MEH,KWY,KWZ,LZO | Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, se Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium phosphate,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented | 2 | Avenir® | |
26 | 00889024491953 | 02.02261.313 | HWC,HRS | Screw, fixation, bone,Plate, fixation, bone | 2 | NCB® | ||
27 | 00889024487734 | 01.03791.070 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Zimmer® DTO® | |||
28 | 00889024303010 | 75.13.33 | 75.13.33 | HTF | CURETTE | 1 | N/A | |
29 | 00889024485044 | 01.03791.060 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Zimmer® DTO® | |||
30 | 00889024485037 | 01.03791.050 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Zimmer® DTO® | |||
31 | 00889024485020 | 01.03791.040 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Zimmer® DTO® | |||
32 | 00889024590830 | 01.06010.206 | 01.06010.206 | LZO,KWL,LWJ,KWZ,KWY | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Avenir® Müller | |
33 | 00889024484832 | 01.04211.183 | 01.04211.183 | PHX,HSD,KWS,KWT | shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, HEMI-, HUMERAL, shoulder prosthesis, reverse configuration,PROSTHESIS, SHOULDER, HEMI-, HUMERAL, METALLIC UNCEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED | 2 | Anatomical Shoulder™ | |
34 | 00889024482920 | 01.00551.308 | 01.00551.308 | KWZ,LWJ,KWY,JDI,KWL,LZO | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented | 2 | Fitmore® | |
35 | 00889024482906 | 01.00551.306 | 01.00551.306 | KWL,JDI,LWJ,LZO,KWZ,KWY | Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/ Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Fitmore® | |
36 | 00889024482777 | 01.00551.107 | 01.00551.107 | KWL,KWZ,LZO,JDI,LWJ,KWY | Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, constrained, cemented or Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Fitmore® | |
37 | 00889024479791 | 01.03715.235 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
38 | 00889024470811 | 01.00555.210 | 01.00555.210 | KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Fitmore | |
39 | 00889024470804 | 01.00555.209 | 01.00555.209 | KWY | Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Fitmore | |
40 | 00889024590755 | 01.06010.302 | 01.06010.302 | KWL,LZO,KWZ,LWJ,KWY | Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/ Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented | 2 | Avenir® Müller | |
41 | 00889024482685 | 01.00551.111 | 01.00551.111 | KWZ,KWY,JDI,LWJ,KWL,LZO | Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented | 2 | Fitmore® | |
42 | 00889024482470 | 01.03717.255 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
43 | 00889024482449 | 01.03717.240 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
44 | 00889024482432 | 01.03717.235 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
45 | 00889024482364 | 01.03716.045 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
46 | 00889024482333 | 01.00296.200 | JDL,LPH,LZO,LWJ,JDI,KWL,KWZ,KWA | Prosthesis, hip, semi-constrained (metal cemented acetabular component),PROSTHES Prosthesis, hip, semi-constrained (metal cemented acetabular component),PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, semi-constrained (metal uncemented acetabular component) | 2 | CLS® Brevius® Kinectiv® | ||
47 | 00889024482272 | 01.00296.125 | JDI,KWA,KWZ,LZO,KWL,LWJ,LPH,JDL | Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained (metal uncemented acetabular component),Prosthesis, hip, constrained, cemented or uncemented, metal/polymer,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, hemi-, femoral, metal,Prosthesis, hip, semi-constrained, metal/polymer, uncemented,PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained (metal cemented acetabular component) | 2 | CLS® Brevius® Kinectiv® | ||
48 | 00889024482234 | 01.03758.055 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
49 | 00889024482180 | 01.03757.255 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® | |||
50 | 00889024482166 | 01.03757.245 | NQP | POSTERIOR METAL/POLYMER SPINAL SYSTEM, FUSION | Dynesys® |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 15060155711260 | 234-010-173 | 234-010-173 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
2 | 15060155711253 | 234-010-172 | 234-010-172 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
3 | 15060155711246 | 234-010-168 | 234-010-168 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
4 | 15060155711239 | 234-010-170 | 234-010-170 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
5 | 15060155711222 | 234-010-160 | 234-010-160 | The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorba The Biosteon® ACL Screw is a cannulated, single-use bone screw made of a resorbable Poly (L-lactic) Acid and Calcium Phosphate which will be gradually resorbed into the body. this function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
6 | 15060155711215 | 3910-200-086 | 3910-200-086 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
7 | 15060155711208 | 3910-200-085 | 3910-200-085 | The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 6.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
8 | 15060155711192 | 3910-200-084 | 3910-200-084 | The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 6.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
9 | 15060155711185 | 3910-200-083 | 3910-200-083 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with three #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
10 | 15060155711178 | 3910-200-082 | 3910-200-082 | The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force F The Biosteon® IntraLine® 5.5mm HA/PLLA Needled Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with stainless steel needles and polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
11 | 15060155711161 | 3910-200-081 | 3910-200-081 | The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, i The Biosteon® IntraLine® 5.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
12 | 15060155711154 | 3910-200-080 | 3910-200-080 | The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is The Biosteon® IntraLine 4.5mm HA/PLLA Suture Anchor with two #2 Force Fibre®, is a single use device. It is made from a resorbable composite which will gradually be resorbed into the body. This function however is patient dependent. The device is supplied sterile. The device is intended to secure a suture or sutures to bone that are then used to reattach damaged soft tissue in orthopaedic procedures in the shoulder, foot/ankle, knee, hand/wrist, elbow and pelvis. The device is supplied with polyethylene sutures. | Biosteon® IntraLine® | BIOCOMPOSITES LTD |
13 | 15060155710652 | 160-135T | 160-135T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
14 | 15060155710645 | 160-130T | 160-130T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
15 | 15060155710621 | 160-935T | 160-935T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
16 | 15060155710614 | 160-930T | 160-930T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
17 | 15060155710607 | 160-925T | 160-925T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
18 | 15060155710584 | 160-830T | 160-830T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
19 | 15060155710577 | 160-825T | 160-825T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible. | Bilok® Screw | BIOCOMPOSITES LTD |
20 | 15060155710546 | 160-725T | 160-725T | The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of The Bilok® Tapered Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok° Screw provides an interference fixation during femoral and/or tibial fixation in ACL reconstruction that resorbs and is replaced with bone during the healing process. Bilok® Screws are biodegradable and biocompatible and should not be used at an infected site. | Bilok® Screw | BIOCOMPOSITES LTD |
21 | 15060155710508 | 160-935ST | 160-935ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
22 | 15060155710492 | 160-930ST | 160-930ST | The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an a The Bilok® ST Screw is a cannulated, sterile, single-use bone screw made of an absorbable Poly (L-lactic) acid and calcium phosphate which will gradually be absorbed into the body over a period of 24 months. This function however is patient dependant. The Bilok® ST Screw is for use as a fixation screw in cruciate ligament surgery. It provides a combination of suspension and compression fixation that resorbs and it is subsequently replaced with bone during the healing process. Bilok® ST Screw is biodegradable and biocompatible. | Bilok® ST Screw | BIOCOMPOSITES LTD |
23 | 15060155710362 | 234-500-350 | 234-500-350 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
24 | 15060155710355 | 234-500-340 | 234-500-340 | The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction The Biosteon® Cross Pin is a bioabsorbable HA/PLLA, for surgical reconstruction of anterior cruciate ligament (ACL) deficient knee to provide cross pin femoral fixation of the various soft tissue ACL autografts and allografts. | Biosteon® Cross Pin | BIOCOMPOSITES LTD |
25 | 15060155710348 | 234-010-180 | 234-010-180 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
26 | 15060155710331 | 234-010-179 | 234-010-179 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
27 | 15060155710324 | 234-010-178 | 234-010-178 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
28 | 15060155710317 | 234-010-177 | 234-010-177 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
29 | 15060155710300 | 234-010-167 | 234-010-167 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
30 | 15060155710294 | 234-010-166 | 234-010-166 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
31 | 15060155710287 | 234-010-165 | 234-010-165 | The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL Screw is a cannulated single-use bone screw made of a resorbable Poly (l-lactic) Acid and Calcium Phosphate, which will be gradually resorbed into the body, this function however, is patient dependant. | Biosteon® Screw | BIOCOMPOSITES LTD |
32 | 15060155710270 | 234-010-164 | 234-010-164 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
33 | 15060155710263 | 234-010-163 | 234-010-163 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
34 | 15060155710256 | 234-010-162 | 234-010-162 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
35 | 15060155710249 | 234-010-161 | 234-010-161 | The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbab The Biosteon® ACL screw is a cannulated single-use bone screw made of a resorbable Poly (L-latic) Acid and calcium phosphate which will be gradually resorbed into the body. This function however, is patient dependent. | Biosteon® Screw | BIOCOMPOSITES LTD |
36 | 14061144348987 | GP001A.076.031.MH | GP001A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
37 | 14053613285541 | OC06D.076.032 | OC06D.076.032.STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
38 | 14053613285534 | OC907P.067.032 | OC907P.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
39 | 14053613285329 | GS905.050.032.M5 | GS905.050.032.STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
40 | 14053613285145 | 02-029-99-1004 | 02-029-99-1004 | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
41 | 14053613284780 | GP007.075.032.K4 | GP007.075.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
42 | 14053613284766 | GS901.033.032.K4 | GS901.033.032 | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
43 | 14053613284391 | OC06Z.127.032 | OC06Z.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
44 | 14053613284384 | OC04N.127.032 | OC04N.127.032 STE | GUIDE PIN SET | GEBR. BRASSELER GMBH & CO. KG | |
45 | 14053613284377 | OC06D.067.032 | OC06D.067.032 STE | GUIDE PIN & GUIDE SCREW SET | GEBR. BRASSELER GMBH & CO. KG | |
46 | 14053613284223 | GP007A.076.031 | GP007A.076.031 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
47 | 14053613283837 | OC005.067.032 STE | OC005.067.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
48 | 14053613282625 | GP003A.027.030.M5 | GP003A.027.030 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
49 | 14053613282601 | OC002A.089.032 STE | OC002A.089.032 STE | GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG | |
50 | 14053613282069 | GP005.067.032.M5 | GP005.067.032 STE | KOMET GUIDE PIN/SCREW | GEBR. BRASSELER GMBH & CO. KG |