Primary Device ID | E22110991 |
NIH Device Record Key | c6b4030b-7fdb-41b0-9324-1ebc846bc18d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Provicol QM |
Version Model Number | 1099 |
Catalog Number | 1099 |
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 | 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 |