No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | M711CRT006ST0 | CRT006ST | CP Ti | GWO | Plate, Cranioplasty, Preformed, Alterable | 2 | Neuro & Craniofacial Fixation System | |
2 | M711E20024 | E2002 | E2002 | KWQ,KWP,MNH,MNI,NKB | Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Inte Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease | Excella II® | ||
3 | M711BTA1190 | BTA-119 | Al, SST, Nylon, Silicone | LXH | Orthopedic Manual Surgical Instrument | 1 | PSO | |
4 | M711X212163200 | X21216320 | X21216320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
5 | M711X212163000 | X21216300 | X21216300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
6 | M711X212162800 | X21216280 | X21216280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
7 | M711X212153200 | X21215320 | X21215320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
8 | M711X212153000 | X21215300 | X21215300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
9 | M711X212152800 | X21215280 | X21215280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
10 | M711X212143200 | X21214320 | X21214320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
11 | M711X212143000 | X21214300 | X21214300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
12 | M711X212142800 | X21214280 | X21214280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
13 | M711X212133200 | X21213320 | X21213320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
14 | M711X212133000 | X21213300 | X21213300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
15 | M711X212132800 | X21213280 | X21213280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
16 | M711X212123200 | X21212320 | X21212320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
17 | M711X212123000 | X21212300 | X21212300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
18 | M711X212122800 | X21212280 | X21212280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
19 | M711X212113200 | X21211320 | X21211320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
20 | M711X212113000 | X21211300 | X21211300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
21 | M711X212112800 | X21211280 | X21211280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
22 | M711X212103200 | X21210320 | X21210320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
23 | M711X212103000 | X21210300 | X21210300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
24 | M711X212102800 | X21210280 | X21210280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
25 | M711X212093200 | X21209320 | X21209320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
26 | M711X212093000 | X21209300 | X21209300 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
27 | M711X212092800 | X21209280 | X21209280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
28 | M711X212082800 | X21208280 | X21208280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
29 | M711X210162550 | X21016255 | X21016255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
30 | M711X210162500 | X21016250 | X21016250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
31 | M711X210162250 | X21016225 | X21016225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
32 | M711X210162200 | X21016220 | X21016220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
33 | M711X210153200 | X21015320 | X21015320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
34 | M711X210152800 | X21015280 | X21015280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
35 | M711X210152550 | X21015255 | X21015255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
36 | M711X210152500 | X21015250 | X21015250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
37 | M711X210152250 | X21015225 | X21015225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
38 | M711X210152200 | X21015220 | X21015220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
39 | M711X210143200 | X21014320 | X21014320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
40 | M711X210142800 | X21014280 | X21014280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
41 | M711X210142550 | X21014255 | X21014255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
42 | M711X210142500 | X21014250 | X21014250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
43 | M711X210142250 | X21014225 | X21014225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
44 | M711X210142200 | X21014220 | X21014220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
45 | M711X210133200 | X21013320 | X21013320 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
46 | M711X210132800 | X21013280 | X21013280 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
47 | M711X210132550 | X21013255 | X21013255 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
48 | M711X210132500 | X21013250 | X21013250 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
49 | M711X210132250 | X21013225 | X21013225 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
50 | M711X210132200 | X21013220 | X21013220 | PEEK, Ta | MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | 2 | Px™ |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 04546540718815 | 234-200-112 | 234-200-112 | ANGLED PEAR CURETTE, LONG | NA | STRYKER CORPORATION |
2 | 04546540718808 | 234-200-111 | 234-200-111 | ANGLED REVERSE TRIANGLE CURETTE, LONG | NA | STRYKER CORPORATION |
3 | 04546540718792 | 234-200-110 | 234-200-110 | ANGLED RING CURETTE, LONG | NA | STRYKER CORPORATION |
4 | 04546540718754 | 234-200-012 | 234-200-012 | ANGLED PEAR CURETTE | NA | STRYKER CORPORATION |
5 | 04546540718747 | 234-200-011 | 234-200-011 | ANGLED REVERSE TRIANGLE CURETTE | NA | STRYKER CORPORATION |
6 | 04046964816697 | ME185R | ME185R | REVERSE ANGLE CUP CURETTE 60°, 5.2MMX7.3 | AESCULAP | AESCULAP IMPLANT SYSTEMS, LLC |
7 | 04046964275715 | ME643R | ME643R | A-SPACE SIBD Bone Curette, 45 °, angled, sharp, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
8 | 04046964275708 | ME642R | ME642R | A-SPACE SIBD Bone Curette, 60 °, reverse angled, sharp, 7,5 x 9 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
9 | 04046964275395 | ME641R | ME641R | A-SPACE SIBD Bone Curette, 60 °, reverse angled, sharp, 5,2 x 7,3 mm, non-steril A-SPACE SIBD Bone Curette, 60 °, reverse angled, sharp, 5,2 x 7,3 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
10 | 04046964275388 | ME644R | ME644R | A-SPACE SIBD Bone Curette, 0 °, straight, sharp, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
11 | 04046963975661 | ME626R | ME626R | A-SPACE SIBD Box Curette, 30 °, angled, 14 x 13,8 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
12 | 04046963975654 | ME625R | ME625R | A-SPACE SIBD Box Curette, 0 °, straight, 14 x 13,8 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
13 | 04046963975647 | ME624R | ME624R | A-SPACE SIBD Curette, teardrop, sharp, small, 8,3 x 19 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
14 | 04046963975630 | ME623R | ME623R | A-SPACE SIBD Ring Curette, 0 °, straight, diam. 10 mm, sharp, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
15 | 04046963975623 | ME622R | ME622R | A-SPACE SIBD Ring Curette, 45 °, angled, diam. 10 mm, sharp, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
16 | 04046963975616 | ME621R | ME621R | A-SPACE SIBD Bone Curette, 45 °, angled, 5 x 9 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
17 | 04046963975609 | ME620R | ME620R | A-SPACE SIBD Bone Curette, 30 °, angled, 5,2 x 7,3 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
18 | 04046963975593 | ME619R | ME619R | A-SPACE SIBD Bone Curette, 0 °, straight, 5 x 9 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
19 | 04046963975586 | ME618R | ME618R | A-SPACE SIBD Bone Curette, 0 °, straight, 5,2 x 7,3 mm, non-sterile, reusable | A-SPACE SIBD | AESCULAP AG |
20 | 04046963129958 | FW872R | FW872R | ACTIV C Curette, teardrop, width: 4,500 mm, non-sterile, reusable | ACTIV C | AESCULAP AG |
21 | 04046963120047 | FK850SU | FK850SU | SUSI Bone Curette, 7", (180 mm), double ended, sharp, sterile, disposable, pack SUSI Bone Curette, 7", (180 mm), double ended, sharp, sterile, disposable, pack of 20 pcs, single packed | SUSI | AESCULAP AG |
22 | 03663136026282 | U1-A123L | Curette | P.L.U.S.® | SPINEVISION | |
23 | 03663136024714 | U1 - A123LSH | CURETTE with silicone handle | P.L.U.S.® | SPINEVISION | |
24 | 03663136024707 | U1-A123 | CURETTE | P.L.U.S.® | SPINEVISION | |
25 | 03663136024424 | TL1-A021 | Straight downbiting curette | NA | SPINEVISION | |
26 | 03663136024370 | TL1-A017-2 | Angled curette right | NA | SPINEVISION | |
27 | 03663136024363 | TL1-A017-1 | Angled curette left | NA | SPINEVISION | |
28 | 03663136024356 | TL1-A016 | Straight rack curette | NA | SPINEVISION | |
29 | 03613720225317 | MS6010042 | SMALL CURETTE | IMPIX-C | MEDICREA INTERNATIONAL | |
30 | 03613720225300 | MS6010041 | LARGE CURETTE | IMPIX-L | MEDICREA INTERNATIONAL | |
31 | 03613720224785 | MS505 | LAMINAR AND TRANSVERSE PROCESS HOOK STARTER | PASS LP | MEDICREA INTERNATIONAL | |
32 | 03613720224778 | MS5054 | PEDICLE HOOK STARTER | PASS LP | MEDICREA INTERNATIONAL | |
33 | 03613720216070 | A15000414 | STRAIGHT CUPPED CURETTE | TAP-LIF Instruments | MEDICREA INTERNATIONAL | |
34 | 03613720216063 | A15000413 | RIGHT BENT CUPPED CURETTE | TAP-LIF Instruments | MEDICREA INTERNATIONAL | |
35 | 03613720216056 | A15000412 | LEFT BENT CUPPED CURETTE | TAP-LIF Instruments | MEDICREA INTERNATIONAL | |
36 | 03613720215950 | A15000402 | BENT CURETTE | TAP-LIF Instruments | MEDICREA INTERNATIONAL | |
37 | 03613720215943 | A15000401 | STRAIGHT CURETTE | TAP-LIF Instruments | MEDICREA INTERNATIONAL | |
38 | 03613720212171 | A02240020 | LAMINAR AND TRANSVERSE PROCESS HOOK STARTER | PASS LP | MEDICREA INTERNATIONAL | |
39 | 00889795111340 | P99-150-0098 | P99-150-0098 | Curette, 9mm, 45 Degrees | APEX 3D Total Ankle Replacement System | PARAGON 28, INC. |
40 | 00889795054364 | P99-150-0135 | P99-150-0135 | Bone Fenestration Chisel, Curved | Multi System | PARAGON 28, INC. |
41 | 00889795054302 | P99-150-0097 | P99-150-0097 | Curette, 20° Angled, 7mm | Multi System | PARAGON 28, INC. |
42 | 00889795054296 | P99-150-0096 | P99-150-0096 | Curette, Curved, 7mm | Multi System | PARAGON 28, INC. |
43 | 00889795054289 | P99-150-0095 | P99-150-0095 | Curette, Ring, Straight, 7mm | Multi System | PARAGON 28, INC. |
44 | 00889795054272 | P99-150-0094 | P99-150-0094 | Curette, Ring, 20° Angled, 7mm | Multi System | PARAGON 28, INC. |
45 | 00889795041050 | P99-150-0091 | P99-150-0091 | Mini Curette, Large, 20° | Baby Gorilla/Gorilla Plating System | PARAGON 28, INC. |
46 | 00889795041043 | P99-150-0090 | P99-150-0090 | Mini Curette, Small, 20° | Baby Gorilla/Gorilla Plating System | PARAGON 28, INC. |
47 | 00889024376649 | 5049-55-10 | Quik-Use® | ZIMMER, INC. | ||
48 | 00889024376632 | 5049-55 | Quik-Use® | ZIMMER, INC. | ||
49 | 00889024376625 | 5049-53 | Quik-Use® | ZIMMER, INC. | ||
50 | 00889024303218 | 75.51.92 | 75.51.92 | N/A | ZIMMER GMBH |