| Primary Device ID | 04251366911059 |
| NIH Device Record Key | d4feff2a-84bc-42c2-9cf5-b74a7da386b9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | priti®multidisc ZrO2 |
| Version Model Number | 13107-D985-30A4T |
| 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 | 04251366911059 [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 | 2023-05-17 |
| Device Publish Date | 2023-05-09 |
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 |