Primary Device ID | 00883205105905 |
NIH Device Record Key | 5edf8c3b-30fc-4d9b-a215-d9dd9cad6f47 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Consepsis |
Version Model Number | 687 |
Catalog Number | 687 |
Company DUNS | 013369913 |
Company Name | ULTRADENT PRODUCTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 |
Storage Environment Temperature | Between 18 Degrees Celsius and 29 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883205105905 [Primary] |
LBH | VARNISH, CAVITY |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-05 |
Device Publish Date | 2016-09-22 |
00883205106704 | Consepsis Bottle 16oz |
00883205106322 | Consepsis V IndiSpense Refill |
00883205105912 | Consepsis Scrub IndiSpense Refill |
00883205105905 | Consepsis IndiSpense Refill |
00883205105820 | Consepsis Scrub IndiSpense Kit |
00883205105615 | Consepsis IndiSpense Kit |
00883205103789 | Consepsis Scrub Kit |
00883205103772 | Consepsis Scrub Refill |
00883205103581 | Consepsis Kit |
00883205102669 | Consepsis Econo Refill |
00883205102607 | Consepsis Unit Dose 50pk |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CONSEPSIS 74404593 1824882 Live/Registered |
Ultradent Products, Inc. 1993-06-18 |