Primary Device ID | 07899633825806 |
NIH Device Record Key | fbd69363-af6f-4b03-9b76-68957ad5f8ed |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Allcem Veneer Try-in |
Version Model Number | OW 2g |
Company DUNS | 898067533 |
Company Name | Dentscare Ltda |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07899633825806 [Primary] |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-06-08 |
Device Publish Date | 2020-05-31 |
07899633825806 | 4000055059 - ALLCEM VENEER TRY IN OW 2G CE FDA |
07899633825790 | 4000055060 - ALLCEM VENEER TRY IN TRANS 2G CE FDA |
07899633825783 | 4000055057 - ALLCEM VENEER TRYIN E BLEACH M 2G CE FDA |
07899633825776 | 4000055065 - ALLCEM VENEER TRY IN A2 2G CE FDA |
07899633825653 | 4000055052 - ALLCEM VENEER TRY IN A1 2G CE FDA |
07899633825646 | 4000055051 - ALLCEM VENEER TRY IN A3 2G CE FDA |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ALLCEM VENEER TRY-IN 88275199 not registered Live/Pending |
DENTSCARE LTDA. 2019-01-24 |
ALLCEM VENEER TRY-IN 88275195 not registered Live/Pending |
DENTSCARE LTDA. 2019-01-24 |