Primary Device ID | 00841036272432 |
NIH Device Record Key | 468a1e70-8fb1-4916-aeea-948f1a7537ef |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | 323.1203 |
Catalog Number | 323.1203 |
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 |