Skini Syringe 1880

GUDID 00883205004598

Skini Syringe Clear 20pk

ULTRADENT PRODUCTS, INC.

General-purpose syringe, single-use
Primary Device ID00883205004598
NIH Device Record Key00e9e5b8-e53b-4710-9c87-b095c5611fa3
Commercial Distribution StatusIn Commercial Distribution
Brand NameSkini Syringe
Version Model Number1880
Catalog Number1880
Company DUNS013369913
Company NameULTRADENT PRODUCTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com
Phone+1(801)572-4200
Emailcustomerservice@ultradent.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100883205004598 [Primary]

FDA Product Code

EICSYRINGE, PERIODONTIC, ENDODONTIC, IRRIGATING

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-12-16
Device Publish Date2024-12-07

On-Brand Devices [Skini Syringe]

00883205019578Skini Syringes 20pk
00883205004871Skini Syringes 50pk
00883205004598Skini Syringe Clear 20pk

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