Primary Device ID | 00883205106711 |
NIH Device Record Key | 4e6551d4-d8ac-4b8b-ae08-5dd6f8da8d6a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EDTA |
Version Model Number | 4616 |
Catalog Number | 4616 |
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 | 00883205106711 [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 | 2018-07-06 |
Device Publish Date | 2017-08-10 |
00883205106711 | EDTA 18% Bottle 16oz |
00883205105431 | EDTA 18% Solution IndiSpense Refill |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EDTA 76311786 2653968 Live/Registered |
Educational Theatre Association 2001-09-14 |
EDTA 73098667 1071704 Dead/Cancelled |
Atomic Products Corp. 1976-09-02 |