| Primary Device ID | 20789594000989 |
| NIH Device Record Key | 4623f980-042b-4e46-b8f1-98f282ac1aeb |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Micro-Stix |
| Version Model Number | 291784 |
| 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 | 00789594000985 [Primary] |
| GS1 | 10789594000982 [Package] Contains: 00789594000985 Package: [4 Units] In Commercial Distribution |
| GS1 | 20789594000989 [Package] Contains: 10789594000982 Package: [350 Units] In Commercial Distribution |
| EJB | HANDLE, INSTRUMENT, DENTAL |
| 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 |
| 20789594000989 | 291784 |
| 20789594000842 | -STIX64B |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MICRO-STIX 86593117 4907486 Live/Registered |
Young Microbrush, LLC 2015-04-10 |
![]() MICRO-STIX 77302203 3607837 Live/Registered |
Young Microbrush, LLC 2007-10-11 |