| Primary Device ID | 00889797102667 |
| NIH Device Record Key | 30487bd7-8fc2-497c-a368-f3222f678008 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | RR100PL |
| Catalog Number | RR100PL |
| Company DUNS | 807201207 |
| Company Name | WRIGHT MEDICAL TECHNOLOGY, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com | |
| Phone | +1(800)238-7117 |
| customerservice@wmt.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889797102667 [Primary] |
| KTT | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
[00889797102667]
Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-04-01 |
| Device Publish Date | 2022-03-24 |
| 00889797104159 - N/A | 2024-10-21 Procedure Pack Sterile |
| 00889797109802 - N/A | 2024-10-15 SOLO™ Proximal Guide Block |
| 00889797109819 - N/A | 2024-10-15 SOLO™ Corner Removal Guide |
| 00889797103923 - PROstep MIS | 2024-09-23 Chamfer Screw |
| 00889797106351 - Made-To-Order | 2024-09-11 Swanson Toe Grommet Seater |
| 00889797107433 - Made-To-Order | 2024-09-11 Inbone® Strike Rod |
| 00889797107457 - Made-To-Order | 2024-09-11 Inbone® Strike Rod |
| 00889797107471 - Made-To-Order | 2024-09-11 Cartilage Removal Tool |