Primary Device ID | 07290109742113 |
NIH Device Record Key | 3c7f4ac8-4801-4680-9a8e-e2e0f751dc5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Straight Multi Unit L=2 |
Version Model Number | 1 |
Catalog Number | BH-MUOOH2 |
Company DUNS | 600330916 |
Company Name | BHI IMPLANTS LTD |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |