Primary Device ID | 00883205103246 |
NIH Device Record Key | 8ac7659b-9191-4f12-9675-19e27a0a3b66 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Opal Bond Flow |
Version Model Number | 500041 |
Catalog Number | 500041 |
Company DUNS | 013369913 |
Company Name | ULTRADENT PRODUCTS, 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 | true |
Device Combination Product | false |
Single Use | false |
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 |