Primary Device ID | 20789594000651 |
NIH Device Record Key | 996ebef8-b147-4540-a1fd-fe3ea0cb9c2b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dri-Aids |
Version Model Number | 331375 |
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 | 00789594000657 [Primary] |
GS1 | 10789594000654 [Package] Contains: 00789594000657 Package: [750 Units] In Commercial Distribution |
GS1 | 20789594000651 [Package] Contains: 10789594000654 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 |