Primary Device ID | 00888233018746 |
NIH Device Record Key | 29933da4-d3de-405a-8c5d-b59f23ff87cd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | SP-2745 |
Catalog Number | SP-2745 |
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 |