| Primary Device ID | 20789594000682 |
| NIH Device Record Key | 80b88c99-8b3f-4ec6-9fdd-1bd3bb54c999 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Dri-Aids |
| Version Model Number | 332325 |
| 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 | 00789594000688 [Primary] |
| GS1 | 10789594000685 [Package] Contains: 00789594000688 Package: [250 Units] In Commercial Distribution |
| GS1 | 20789594000682 [Package] Contains: 10789594000685 Package: [13 Units] In Commercial Distribution |
| KHR | ABSORBER, SALIVA, PAPER |
| 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 |
| 10789594000692 | 332375 |
| 20789594000682 | 332325 |
| 20789594000675 | 332190 |
| 20789594000668 | 332125 |
| 20789594000651 | 331375 |
| 20789594000644 | 331320 |
| 20789594000637 | 331190 |
| 20789594000620 | 331125 |