Primary Device ID | 00840420169303 |
NIH Device Record Key | bdecd13f-09f3-48b4-8937-83b7e2334f8e |
Commercial Distribution Discontinuation | 2016-05-05 |
Commercial Distribution Status | Not in Commercial Distribution |
Version Model Number | 10086 |
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 | |
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 Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840420169303 [Primary] |
KWD | PROSTHESIS, TOE, HEMI-, PHALANGEAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
[00840420169303]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-01-29 |
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 |