Primary Device ID | 00883205106698 |
NIH Device Record Key | 7bed26c3-213f-4924-8ae9-3f02dcc66452 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ChlorCid |
Version Model Number | 4612 |
Catalog Number | 4612 |
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 | 00883205106698 [Primary] |
KJJ | CLEANSER, ROOT CANAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-09-21 |
Device Publish Date | 2017-08-10 |
00883205106698 | ChlorCid Bottle 16oz |
00883205105394 | ChlorCid IndiSpense Refill |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CHLORCID 75122658 2057459 Live/Registered |
Ultradent Products, Inc. 1996-06-20 |