Primary Device ID | DVIV745815AL1 |
NIH Device Record Key | a906a7cf-1e8d-49f2-a9f8-212e9a8b388c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CERVITEC F |
Version Model Number | 745815AL |
Catalog Number | 745815AL |
Company DUNS | 448015938 |
Company Name | IVOCLAR VIVADENT AKTIENGESELLSCHAFT |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |