Primary Device ID | 05414904160770 |
NIH Device Record Key | f7bb6831-9ae6-44d2-bf25-53b644e67272 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CR MD1.0 GENERAL PLATE |
Version Model Number | CR MD1.0 GENERAL PLATE 18X24 |
Catalog Number | 5YEM2 |
Company DUNS | 374444883 |
Company Name | AGFA |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |