Primary Device ID | 00883205021960 |
NIH Device Record Key | 62687edd-3aeb-4348-83c2-1ad12f9dc615 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | STARbrush |
Version Model Number | 1091 |
Catalog Number | 1091 |
Company DUNS | 013369913 |
Company Name | ULTRADENT PRODUCTS, INC. |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(801)572-4200 |
customerservice@ultradent.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883205021960 [Primary] |
EJQ | WHEEL, POLISHING AGENT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-12-21 |
Device Publish Date | 2017-05-23 |
00883205021984 | StarBrushes 100pk |
00883205021977 | StarBrushes 50pk |
00883205021960 | StarBrushes 30pk |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STARBRUSH 78286855 2862935 Live/Registered |
Ultradent Products, Inc. 2003-08-13 |