Primary Device ID | 04251366913817 |
NIH Device Record Key | 07d876c1-427f-4508-a2a7-c8111fcfab0c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | priti®multidisc ZrO2 |
Version Model Number | HZRA3414 |
Company DUNS | 341632902 |
Company Name | Pritidenta 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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04251366913817 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-15 |
Device Publish Date | 2024-08-07 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PRITI 90817047 not registered Live/Pending |
pritidenta GmbH 2021-07-08 |
![]() PRITI 86005224 4598617 Live/Registered |
Joanna Feldheim 2013-07-09 |
![]() PRITI 85052053 not registered Dead/Abandoned |
Paraflex Inc. 2010-06-01 |
![]() PRITI 79206855 5420520 Live/Registered |
pritidenta GmbH 2017-01-12 |
![]() PRITI 79089895 not registered Dead/Abandoned |
pritidenta GmbH 2010-10-13 |
![]() PRITI 77607362 not registered Dead/Abandoned |
Priti Nails LLC 2008-11-04 |
![]() PRITI 76651366 not registered Dead/Abandoned |
Jewelex New York Ltd. 2005-12-05 |