Primary Device ID | 00883205004598 |
NIH Device Record Key | 00e9e5b8-e53b-4710-9c87-b095c5611fa3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Skini Syringe |
Version Model Number | 1880 |
Catalog Number | 1880 |
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 | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com | |
Phone | +1(801)572-4200 |
customerservice@ultradent.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00883205004598 [Primary] |
EIC | SYRINGE, PERIODONTIC, ENDODONTIC, IRRIGATING |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-16 |
Device Publish Date | 2024-12-07 |
00883205019578 | Skini Syringes 20pk |
00883205004871 | Skini Syringes 50pk |
00883205004598 | Skini Syringe Clear 20pk |