Primary Device ID | 00840420117762 |
NIH Device Record Key | e7fb4004-4120-440a-964c-c2abc9e3bcd1 |
Commercial Distribution Discontinuation | 2016-03-07 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | TCP |
Version Model Number | 03-9013-12 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |