Primary Device ID | 00888480165828 |
NIH Device Record Key | 68359e30-ab73-40d6-a255-68aa127c53b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PHOENIX ANTEGRADE NAIL SYSTEM |
Version Model Number | 14-443842 |
Catalog Number | 14-443842 |
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 |