No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00889024464315 | 00-7050-078-00 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | NA | ||
2 | 00889024464292 | 00-7050-076-00 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | NA | ||
3 | 00889024464278 | 00-7050-038-00 | HWR | DRIVER, PROSTHESIS | 1 | NA | ||
4 | 00889024464261 | 00-7050-036-00 | HWR | DRIVER, PROSTHESIS | 1 | NA | ||
5 | 00889024464254 | 00-7361-052-22 | HXB | PROBE | 1 | NA | ||
6 | 00889024464247 | 00-7360-070-28 | HXB | PROBE | 1 | NA | ||
7 | 00889024464230 | 00-7360-068-28 | HXB | PROBE | 1 | NA | ||
8 | 00889024464223 | 00-7360-066-28 | HXB | PROBE | 1 | NA | ||
9 | 00889024464216 | 00-7360-064-28 | HXB | PROBE | 1 | NA | ||
10 | 00889024464209 | 00-7360-062-28 | HXB | PROBE | 1 | NA | ||
11 | 00889024464193 | 00-7360-060-28 | HXB | PROBE | 1 | NA | ||
12 | 00889024464186 | 00-7360-058-28 | HXB | PROBE | 1 | NA | ||
13 | 00889024464179 | 00-7360-056-28 | HXB | PROBE | 1 | NA | ||
14 | 00889024464162 | 00-7360-054-28 | HXB | PROBE | 1 | NA | ||
15 | 00889024464155 | 00-7360-052-28 | HXB | PROBE | 1 | NA | ||
16 | 00889024320635 | 96-701-30001 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | ||
17 | 00889024320628 | 96-701-21161 | 96-701-21161 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | |
18 | 00889024320611 | 96-701-21121 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | ||
19 | 00889024320604 | 96-701-21101 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | ||
20 | 00889024320598 | 96-701-21081 | 96-701-21081 | GAD,MAX | RETRACTOR,Intervertebral fusion device with bone graft, lumbar | 1 | TM Ardis® | |
21 | 00889024320581 | 96-701-20161 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | ||
22 | 00889024320574 | 96-701-20121 | 96-701-20121 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | |
23 | 00889024320567 | 96-701-20101 | 96-701-20101 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | |
24 | 00889024320550 | 96-701-20081 | MAX,GAD | Intervertebral fusion device with bone graft, lumbar,RETRACTOR | 1 | TM Ardis® | ||
25 | 00889024320543 | 96-701-10001 | 96-701-10001 | MAX | Intervertebral fusion device with bone graft, lumbar | 2 | TM Ardis® | |
26 | 00889024320536 | 96-499-60001 | 96-499-60001 | FSM,MQP,MAX | TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebr TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar | 1 | NA | |
27 | 00889024320529 | 96-499-50001 | 96-499-50001 | MQP,MAX,FSM | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
28 | 00889024320505 | 96-499-30001 | 96-499-30001 | MAX,MQP,FSM | Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
29 | 00889024320499 | 96-499-20001 | 96-499-20001 | MQP,MAX,FSM | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT | 1 | NA | |
30 | 00889024320482 | 96-499-10001 | 96-499-10001 | MQP,FSM,MAX | SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebr SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebral fusion device with bone graft, lumbar | 1 | NA | |
31 | 00889024320031 | 96-215-21031 | 96-215-21031 | GAD | RETRACTOR | 1 | NA | |
32 | 00889024320024 | 96-215-21021 | 96-215-21021 | GAD | RETRACTOR | 1 | NA | |
33 | 00889024320017 | 96-215-21011 | 96-215-21011 | GAD | RETRACTOR | 1 | NA | |
34 | 00889024320000 | 96-215-21001 | 96-215-21001 | GAD | RETRACTOR | 1 | NA | |
35 | 00889024319998 | 96-215-20001 | 96-215-20001 | GAD | RETRACTOR | 1 | NA | |
36 | 00889024319981 | 96-215-19011 | 96-215-19011 | GAD | RETRACTOR | 1 | NA | |
37 | 00889024319974 | 96-215-19001 | 96-215-19001 | GAD | RETRACTOR | 1 | NA | |
38 | 00889024319967 | 96-215-18001 | 96-215-18001 | GAD | RETRACTOR | 1 | NA | |
39 | 00889024319950 | 96-215-17011 | 96-215-17011 | GAD | RETRACTOR | 1 | NA | |
40 | 00889024319943 | 96-215-17001 | 96-215-17001 | GAD | RETRACTOR | 1 | NA | |
41 | 00889024319936 | 96-215-16001 | 96-215-16001 | GAD | RETRACTOR | 1 | NA | |
42 | 00889024319929 | 96-215-15011 | 96-215-15011 | GAD | RETRACTOR | 1 | NA | |
43 | 00889024319912 | 96-215-15001 | 96-215-15001 | GAD | RETRACTOR | 1 | NA | |
44 | 00889024319905 | 96-215-14011 | 96-215-14011 | GAD | RETRACTOR | 1 | NA | |
45 | 00889024319899 | 96-215-14001 | 96-215-14001 | GAD | RETRACTOR | 1 | NA | |
46 | 00889024319882 | 96-215-13011 | 96-215-13011 | GAD | RETRACTOR | 1 | NA | |
47 | 00889024319875 | 96-215-13001 | 96-215-13001 | GAD | RETRACTOR | 1 | NA | |
48 | 00889024319868 | 96-215-12011 | 96-215-12011 | GAD | RETRACTOR | 1 | NA | |
49 | 00889024319851 | 96-215-12001 | 96-215-12001 | GAD | RETRACTOR | 1 | NA | |
50 | 00889024319844 | 96-215-11011 | 96-215-11011 | GAD | RETRACTOR | 1 | NA |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 05055313825616 | 6-139 | 6-139 | Component Case | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
2 | 05055313824480 | 6-675-1 | 6-675-1 | Flushing Adaptor | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
3 | 05055313822622 | 6-675 | 6-675 | Flushing Adaptor | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
4 | 05055313818175 | T7020-2 | T7020-2 | Sterilising Tray | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
5 | 05055313818168 | T7020 | T7020 | Sterilising Tray | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
6 | 05055313818113 | T7003-1 | T7003-1 | Sterilising Tray | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
7 | 05055313809104 | 6-135-1 | 6-135-1 | Sterilising Case | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
8 | 05055313809098 | 6-135 | 6-135 | Sterilising Case | Duckworth & Kent | DUCKWORTH AND KENT LIMITED |
9 | 05050474520738 | OM290901 | OM290901 | INSTRUMENT TRAY | NA | JOHNSON & JOHNSON SURGICAL VISION, INC. |
10 | 05019279784325 | 32-421068 | 32-421068 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT TRAY | BIOMET UK LTD | |
11 | 05019279511020 | 32-423534 | 32-423534 | OXFORD MICROPLASTY KNEE SYSTEMFEMORAL INSTRUMENT TRAY | BIOMET UK LTD | |
12 | 05019279511105 | 32-423538 | 32-423538 | OXFORD MICROPLASTY KNEE SYSTEMFEMORAL INSTRUMENT TRAY | BIOMET UK LTD | |
13 | 05019279488636 | 32-420727 | 32-420727 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT CASE | BIOMET UK LTD | |
14 | 05019279488599 | 32-420726 | 32-420726 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT CASE | BIOMET UK LTD | |
15 | 05019279488551 | 32-420725 | 32-420725 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT CASE | BIOMET UK LTD | |
16 | 05019279488513 | 32-420724 | 32-420724 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT CASE | BIOMET UK LTD | |
17 | 05019279488278 | 32-420700 | 32-420700 | OXFORD UNICOMPARTMENTAL KNEE PHASE 3TIBIAL CASE | BIOMET UK LTD | |
18 | 05019279478156 | 32-423600 | 32-423600 | Oxford Microplasty Knee System | BIOMET UK LTD | |
19 | 05019279474332 | 31-601565 | 31-601565 | Taperloc Complete Hip SystemGeneral Instrument Case Only | BIOMET UK LTD | |
20 | 05019279439799 | 32-422785 | 32-422785 | OXFORD MICROPLASTY KNEE | BIOMET UK LTD | |
21 | 05019279107070 | 32-422006 | 32-422006 | OXFORD UNICOMPARTMENTAL KNEE SYSTEMCEMENTLESS INSTRUMENT CASE | BIOMET UK LTD | |
22 | 05019279064908 | 31-600035 | 31-600035 | TAPERLOC HIP INSTRUMENTATIONRASP TRAY | BIOMET UK LTD | |
23 | 05019279054091 | 31-600329 | 31-600329 | BIOMET FRACTURE STEM SYSTEMHEMI-ARTHROPLASTY INSTRUMENT CASE | BIOMET UK LTD | |
24 | 04946329210422 | 07-096-55 | 07-096-55 | Anastomosis Clips and Instruments Case | Anastomosis Clips and Instruments Case | MIZUHO CORPORATION |
25 | 04718005152414 | 595-18328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
26 | 04718005152407 | 595-17328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
27 | 04718005152391 | 595-16328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
28 | 04718005152384 | 595-15328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
29 | 04718005152377 | 595-14328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
30 | 04718005152360 | 595-13328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
31 | 04718005152353 | 595-12328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
32 | 04718005152346 | 595-11328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
33 | 04718005152339 | 595-10328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
34 | 04718005152322 | 595-09328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
35 | 04718005152315 | 595-08328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
36 | 04718005152308 | 595-07328 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
37 | 04718005152292 | 595-18308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
38 | 04718005152285 | 595-17308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
39 | 04718005152278 | 595-16308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
40 | 04718005152261 | 595-15308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
41 | 04718005152254 | 595-14308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
42 | 04718005152247 | 595-13308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
43 | 04718005152230 | 595-12308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
44 | 04718005152223 | 595-11308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
45 | 04718005152216 | 595-10308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
46 | 04718005152209 | 595-09308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
47 | 04718005152193 | 595-08308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
48 | 04718005152186 | 595-07308 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
49 | 04718005152179 | 595-18288 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. | |
50 | 04718005152162 | 595-17288 | PEEK Interbody Fusion Cage | COMET Lumbar Interbody Fusion Cage | BAUI BIOTECH CO. LTD. |