Primary Device ID | EPIS33129PF0 |
NIH Device Record Key | a1cc9f31-4ae8-4df3-98ff-f441b79410da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Femoral Drilling Socket |
Version Model Number | D29 |
Catalog Number | 33129PF |
Company DUNS | 352393402 |
Company Name | Episurf Operations AB |
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 | true |
Manufacturing Date | true |
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 |