| Primary Device ID | 10789594000852 |
| NIH Device Record Key | c51e3872-467e-41b9-8a6c-826306a57c1d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ultrabrush |
| Version Model Number | U2R200 |
| Company DUNS | 929236305 |
| Company Name | YOUNG MICROBRUSH, LLC |
| 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 | 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 | 00789594000855 [Primary] |
| GS1 | 10789594000852 [Package] Contains: 00789594000855 Package: [200 Units] In Commercial Distribution |
| GS1 | 20789594000859 [Package] Package: [24 Units] In Commercial Distribution |
| KXR | APPLICATOR, 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 | 2020-12-16 |
| Device Publish Date | 2020-12-08 |
| 10789594000852 | U2R200 |
| 10789594000838 | U1R200 |
| 10789594000722 | U2D |
| 20789594000712 | U1D |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ULTRABRUSH 75606456 2457972 Live/Registered |
YOUNG MICROBRUSH, LLC 1998-12-16 |
![]() ULTRABRUSH 75112169 not registered Dead/Abandoned |
YOUNG MICROBRUSH, LLC 1996-05-31 |
![]() ULTRABRUSH 74264388 not registered Dead/Abandoned |
GEMTech, Inc. 1992-04-10 |