Primary Device ID | 00841036083892 |
NIH Device Record Key | 3b245525-0b7a-4a23-8ea1-93d8c8e139d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TMS SYSTEM |
Version Model Number | 25-2111 |
Catalog Number | 25-2111 |
Company DUNS | 046189866 |
Company Name | BIOMET MICROFIXATION, 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 | false |
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 |