Primary Device ID | 10789594000722 |
NIH Device Record Key | ae411abd-8abc-4de3-9ba0-90d8dbc436b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ultrabrush |
Version Model Number | U2D |
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 | 00789594000725 [Primary] |
GS1 | 10789594000722 [Package] Contains: 00789594000725 Package: [100 Units] In Commercial Distribution |
GS1 | 20789594000729 [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 |