Primary Device ID | 00880304469761 |
NIH Device Record Key | 9443734a-1cfd-479a-a062-ff95c2a2abdd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COMPREHENSIVE INSTRUMENTATION |
Version Model Number | 405810 |
Catalog Number | 405810 |
Company DUNS | 129278169 |
Company Name | Biomet Orthopedics, LLC |
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 | true |
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 |