Primary Device ID | 00887868096587 |
NIH Device Record Key | e6b0df4a-450b-4a3d-a4b7-2d4c08b69768 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PHOENIX ANTEGRADE NAIL SYSTEM |
Version Model Number | 14-443238 |
Catalog Number | 14-443238 |
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 |