Primary Device ID | 00887868003745 |
NIH Device Record Key | f2b9c5a6-10e8-42e9-a359-eea1b20152af |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BONE SCREW, CORTICAL |
Version Model Number | 1020-55 |
Catalog Number | 102055 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |