Primary Device ID | D7075799350 |
NIH Device Record Key | df44c58b-5a73-4c26-b3b6-952e9c5c6462 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | d SIGN 84 |
Version Model Number | 579935 |
Catalog Number | 579935 |
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 |