Primary Device ID | 00093764602245 |
NIH Device Record Key | 7e24abf3-42e1-4561-a167-f2dce56ab23b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | A&D Medical |
Version Model Number | UT-302 |
Catalog Number | UT-302 |
Company DUNS | 102107927 |
Company Name | A & D Medical |
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 | false |
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 | false |
OTC Over-The-Counter | true |