Primary Device ID | 00841036007140 |
NIH Device Record Key | 6cffc55f-1491-4acd-a427-028816846ce7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | 01-0263 |
Catalog Number | 01-0263 |
Company DUNS | 046189866 |
Company Name | BIOMET MICROFIXATION, INC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 |