Primary Device ID | E22110741 |
NIH Device Record Key | f2cd234b-ce5a-4513-bc97-c92a9217f7e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Provicol QM |
Version Model Number | 1074 |
Catalog Number | 1074 |
Company DUNS | 316699578 |
Company Name | VOCO GmbH |
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 |