No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00889797102520 | RR2000 | RR2000 | KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | NA | |
2 | 00889797102513 | RR1200 | RR1200 | JDW,KTT | PIN, FIXATION, THREADED,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTI PIN, FIXATION, THREADED,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | 2 | NA | |
3 | 00840420163493 | SB170150 | SB170150 | HWC | Screw, fixation, bone | 2 | SALVATION | |
4 | 00840420163486 | SB170145 | SB170145 | HWC | Screw, fixation, bone | 2 | SALVATION | |
5 | 00840420163479 | SB170140 | SB170140 | HWC | Screw, fixation, bone | 2 | SALVATION | |
6 | 00840420163462 | SB170135 | SB170135 | HWC | Screw, fixation, bone | 2 | SALVATION | |
7 | 00840420163455 | SB170130 | SB170130 | HWC | Screw, fixation, bone | 2 | SALVATION | |
8 | 00840420163448 | SB170125 | SB170125 | HWC | Screw, fixation, bone | 2 | SALVATION | |
9 | 00840420163431 | SB170120 | SB170120 | HWC | Screw, fixation, bone | 2 | SALVATION | |
10 | 00840420163400 | SB170105 | SB170105 | HWC | Screw, fixation, bone | 2 | SALVATION | |
11 | 00840420163394 | SB170100 | SB170100 | HWC | Screw, fixation, bone | 2 | SALVATION | |
12 | 00840420163387 | SB017095 | SB017095 | HWC | Screw, fixation, bone | 2 | SALVATION | |
13 | 00840420163363 | SB017085 | SB017085 | HWC | Screw, fixation, bone | 2 | SALVATION | |
14 | 00840420163356 | SB017080 | SB017080 | HWC | Screw, fixation, bone | 2 | SALVATION | |
15 | 00840420163349 | SB017075 | SB017075 | HWC | Screw, fixation, bone | 2 | SALVATION | |
16 | 00840420163332 | SB017070 | SB017070 | HWC | Screw, fixation, bone | 2 | SALVATION | |
17 | 00840420163325 | SB017065 | SB017065 | HWC | Screw, fixation, bone | 2 | SALVATION | |
18 | 00840420163301 | SB017055 | SB017055 | HWC | Screw, fixation, bone | 2 | SALVATION | |
19 | 00840420163295 | SB017050 | SB017050 | HWC | Screw, fixation, bone | 2 | SALVATION | |
20 | 00840420197535 | 03-5010 | 03-5010 | RX-FIX Mini Rail System | HWR | DRIVER, PROSTHESIS | 1 | NA |
21 | 00840420197528 | 03-5009 | 03-5009 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
22 | 00840420197511 | 03-5007 | 03-5007 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
23 | 00840420197504 | 03-5005 | 03-5005 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
24 | 00840420197498 | 03-5004 | 03-5004 | T-Tool for Rx-Fix | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA |
25 | 00840420197481 | 03-5002 | 03-5002 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
26 | 00840420197474 | 03-5000 | 03-5000 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
27 | 00840420198808 | 4940125 | KWI | PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER | 2 | NA | ||
28 | 00840420198792 | 4940115 | KWI | PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER | 2 | NA | ||
29 | 00840420198785 | 4940103 | KWI | PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER | 2 | NA | ||
30 | 00840420198778 | 4940102 | KWI | PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER | 2 | NA | ||
31 | 00840420198761 | 4940101 | KWI | PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYMER | 2 | NA | ||
32 | 00840420197566 | 03-5015 | 03-5015 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
33 | 00840420199522 | 8661000 | 8661000 | Trapezium Sizing Set | HWT | Template | 1 | TIE-IN |
34 | 00840420197559 | 03-5013 | 03-5013 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA | |
35 | 00840420163417 | SB170110 | SB170110 | HWC | Screw, fixation, bone | 2 | SALVATION | |
36 | 00840420199720 | 18770140 | 18770140 | Pin Puller | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | NA |
37 | 00840420195425 | FFHSIZER | FFHSIZER | Staple Sizer | HWT | TEMPLATE | 1 | FUSEFORCE™ |
38 | 00840420194848 | SMN10011 | SMN10011 | Step Drill | HTW | BIT, DRILL | 1 | SALVATION |
39 | 00840420194831 | SMN10010 | SMN10010 | Drill | HTW | BIT, DRILL | 1 | SALVATION |
40 | 00840420194824 | SMN10009 | SMN10009 | Quick Connector Inserter | MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE | 1 | SALVATION |
41 | 00840420194817 | SMN10008 | SMN10008 | Implant Holder Assembly | MDM | INSTRUMENT, MANUAL, SURGICAL, GENERAL USE | 1 | SALVATION |
42 | 00840420194800 | SMN10007 | SMN10007 | Targeting Guide Assembly | FZX | Guide, surgical, instrument | 1 | SALVATION |
43 | 00840420194657 | 60006024 | 60006024 | Dome Impaction Block | HWA | IMPACTOR | 1 | INVISION |
44 | 00840420194534 | IB220705 | IB220705 | HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | INVISION | |
45 | 00840420194527 | IB220704 | IB220704 | HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | INVISION | |
46 | 00840420194510 | IB220703 | IB220703 | HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | INVISION | |
47 | 00840420194503 | IB220702 | IB220702 | HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | INVISION | |
48 | 00840420194497 | IB220701 | IB220701 | HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | INVISION | |
49 | 00840420194435 | 60011150 | 60011150 | Talar Plate Trial | HSN | PROSTHESIS, ANKLE, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | INVISION |
50 | 00840420194428 | 60011140 | 60011140 | Talar Plate Trial | HWT | TEMPLATE | 1 | INVISION |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00887868284854 | 348014 | 348014 | Calcigen® S Bone Graft System | BIOMET BIOLOGICS, LLC | |
2 | 00887868284847 | 348012 | 348012 | Calcigen® S Bone Graft System | BIOMET BIOLOGICS, LLC | |
3 | 00887868284830 | 348010 | 348010 | Calcigen® S Bone Graft System | BIOMET BIOLOGICS, LLC | |
4 | 00887517971586 | 5020408994 | Propel DBM Gel Plus, 8cc OUS | Propel | NUVASIVE, INC. | |
5 | 00887517971579 | 5020408 | Propel DBM Gel Plus, 8cc | Propel | NUVASIVE, INC. | |
6 | 00887517971562 | 5020403994 | Propel DBM Gel Plus, 3cc OUS | Propel | NUVASIVE, INC. | |
7 | 00887517971555 | 5020403 | Propel DBM Gel Plus, 3cc | Propel | NUVASIVE, INC. | |
8 | 00887517971548 | 5020401994 | Propel DBM Gel Plus, 1cc OUS | Propel | NUVASIVE, INC. | |
9 | 00887517971531 | 5020401 | Propel DBM Gel Plus, 1cc | Propel | NUVASIVE, INC. | |
10 | 00887517971524 | 5020310994 | Propel DBM Gel, 10cc OUS | Propel | NUVASIVE, INC. | |
11 | 00887517971517 | 5020310 | Propel DBM Gel, 10cc | Propel | NUVASIVE, INC. | |
12 | 00887517971500 | 5020305994 | Propel DBM Gel, 5cc OUS | Propel | NUVASIVE, INC. | |
13 | 00887517970497 | 5020305 | Propel DBM Gel, 5cc | Propel | NUVASIVE, INC. | |
14 | 00887517970480 | 5020301994 | Propel DBM Gel, 1cc OUS | Propel | NUVASIVE, INC. | |
15 | 00887517970473 | 5020301 | Propel DBM Gel, 1cc | Propel | NUVASIVE, INC. | |
16 | 00887517970466 | 5020210994 | Propel DBM Putty Plus, 10cc OUS | Propel | NUVASIVE, INC. | |
17 | 00887517970459 | 5020210 | Propel DBM Putty Plus, 10cc | Propel | NUVASIVE, INC. | |
18 | 00887517970442 | 5020205994 | Propel DBM Putty Plus, 5cc OUS | Propel | NUVASIVE, INC. | |
19 | 00887517970435 | 5020205 | Propel DBM Putty Plus, 5cc | Propel | NUVASIVE, INC. | |
20 | 00887517940025 | 5015102 | AttraX Scaffold Strips, Large | AttraX | NUVASIVE, INC. | |
21 | 00887517940018 | 5015101 | AttraX Scaffold Strips, Small | AttraX | NUVASIVE, INC. | |
22 | 00887517940001 | 5015106 | AttraX Scaffold Blocks, Extra Large | AttraX | NUVASIVE, INC. | |
23 | 00887517939999 | 5015104 | AttraX Scaffold Blocks, Large | AttraX | NUVASIVE, INC. | |
24 | 00887517939982 | 5015103 | AttraX Scaffold Blocks, Small | AttraX | NUVASIVE, INC. | |
25 | 00887517939975 | 5015130 | AttraX Scaffold Morsels, 30cc | AttraX | NUVASIVE, INC. | |
26 | 00887517939968 | 5015120 | AttraX Scaffold Morsels, 20cc | AttraX | NUVASIVE, INC. | |
27 | 00887517939951 | 5015110 | AttraX Scaffold Morsels, 10cc | AttraX | NUVASIVE, INC. | |
28 | 00887517614384 | 5020010 | Propel Putty, Large | Propel | NUVASIVE, INC. | |
29 | 00887517614377 | 5020005 | Propel Putty, Medium | Propel | NUVASIVE, INC. | |
30 | 00887517614360 | 5020001 | Propel Putty, Small | Propel | NUVASIVE, INC. | |
31 | 00887517241566 | 5015010 | AttraX® Putty, 10cc US | AttraX | NUVASIVE, INC. | |
32 | 00887517241559 | 5015006 | AttraX® Putty, 6cc US | AttraX | NUVASIVE, INC. | |
33 | 00887517241542 | 5015005 | AttraX® Putty, 5cc US | AttraX | NUVASIVE, INC. | |
34 | 00887517241535 | 5015002 | AttraX® Putty, 2cc US | AttraX | NUVASIVE, INC. | |
35 | 00887517241528 | 5015001 | AttraX® Putty, 1cc US | AttraX | NUVASIVE, INC. | |
36 | 00887517239372 | 5010205 | FormaGraft® Strips, Small | FormaGraft | NUVASIVE, INC. | |
37 | 00887517239365 | 5010200 | FormaGraft® Strips, Large | FormaGraft | NUVASIVE, INC. | |
38 | 00887517239310 | 5010125 | FormaGraft® XL Blocks, Large | FormaGraft | NUVASIVE, INC. | |
39 | 00887517238450 | 5010085 | FormaGraft® XL Blocks, Small | FormaGraft | NUVASIVE, INC. | |
40 | 00887517238443 | 5010020 | FormaGraft® Granules, 20cc | FormaGraft | NUVASIVE, INC. | |
41 | 00887517238436 | 5010010 | FormaGraft® Granules, 10cc | FormaGraft | NUVASIVE, INC. | |
42 | 00887517238429 | 5010008 | FormaGraft BMA Needle, 8" Packaged | FormaGraft | NUVASIVE, INC. | |
43 | 00887517238412 | 5010005 | FormaGraft® Granules, 5cc | FormaGraft | NUVASIVE, INC. | |
44 | 00887517237392 | 5010001 | FormaGraft BMA Needle, 6-Port (1) | FormaGraft | NUVASIVE, INC. | |
45 | ECURCOM2550 | 25x50x4 mm | 1 x 5.0 cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
46 | ECURCOM2525 | 25x25x2 mm | 1 x 2.5 cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
47 | ECURCOM2512 | 25x12x4 mm | 1 x 1.2 cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
48 | ECURCOM25100 | 25x100x4 mm | 1 x 10.0cc | Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use: Device Name: CERASORB® Ortho FoamMofidication: Mouldable FoamIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
49 | ECURCOF6565 | 65x65x6 mm | 1 x 25.0 cc | Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |
50 | ECURCOF2550 | 25x50x4 mm | 1 x 0.5 cc | Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication fo Device Name: CERASORB® Ortho FoamMofidication: Flexible Foam StripeIndication for Use:Cerasorb® ORTHO Foam is an implant intended to fill bony voids or gaps of the skeletal system (i.e., extremities and pelvis). These osseous defects are surgically created or the result of traumatic injury to the bone and are not intrinsic to the stability of the bony structure. Cerasorb® Ortho Foam resorbs and is replaced with bone during healing process. | CERASORB® Ortho Foam | CURASAN AG |