Primary Device ID | D7075799370 |
NIH Device Record Key | b5a16d1e-9c31-441a-ab7c-6a90c124c14a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | d SIGN 91 |
Version Model Number | 579937 |
Catalog Number | 579937 |
Company DUNS | 176935203 |
Company Name | IVOCLAR VIVADENT, INC. |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |