Primary Device ID | 00026072025048 |
NIH Device Record Key | ffb58297-0b57-4570-8161-702536bd8629 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GM |
Version Model Number | 01-90-8820 |
Company DUNS | 119066872 |
Company Name | Allied Medical, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |