Primary Device ID | 05019279796472 |
NIH Device Record Key | 31d57237-9fb6-4719-8a10-b419f441c550 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MAXIM KNEE INSTRUMENTATION |
Version Model Number | 32-379660 |
Catalog Number | 32-379660 |
Company DUNS | 219322575 |
Company Name | Biomet Uk Ltd |
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 |