Primary Device ID | 00810012483773 |
NIH Device Record Key | 148cdd51-54bb-41e8-9fc6-6e8b7abd1ab1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DRILL GUIDE 7 9MM |
Version Model Number | 17648 |
Company DUNS | 618749857 |
Company Name | BIOPRO, INC. |
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 | 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 |