Black Mini Tip 196

GUDID 00883205021663

Black Mini Tips 20pk

ULTRADENT PRODUCTS, INC.

Surgical/emergency suction cannula, non-illuminating, single-use
Primary Device ID00883205021663
NIH Device Record Key2b6448a5-54cd-4ffb-827e-d22e8c49dc00
Commercial Distribution StatusIn Commercial Distribution
Brand NameBlack Mini Tip
Version Model Number196
Catalog Number196
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
GS100883205021663 [Primary]

FDA Product Code

EIDSYRINGE, RESTORATIVE AND IMPRESSION MATERIAL

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 [Black Mini Tip]

00883205022363Black Mini Tips 500pk
00883205021786Black Mini Tips 100pk
00883205021663Black Mini Tips 20pk

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