Primary Device ID | 00887868033896 |
NIH Device Record Key | d2fbf87b-5827-44cd-9a7d-6f82bbbb4c3e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BONE SCREW, CORTICAL |
Version Model Number | 8050-55-030 |
Catalog Number | 805055030 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |