NaviTip 31G Sideport 5122

GUDID 00883205022837

NaviTip 31g 21mm Sideport 50PK (Yellow)

ULTRADENT PRODUCTS, INC.

Syringe tip cap
Primary Device ID00883205022837
NIH Device Record Keyc4ff04e9-59aa-49a2-a4d8-011b65dc0988
Commercial Distribution StatusIn Commercial Distribution
Brand NameNaviTip 31G Sideport
Version Model Number5122
Catalog Number5122
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100883205022837 [Primary]

FDA Product Code

EICSYRINGE, PERIODONTIC, ENDODONTIC, IRRIGATING

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2017-07-26

On-Brand Devices [NaviTip 31G Sideport]

00883205022851NaviTip 31g 27mm Sideport 50PK (Green)
00883205022844NaviTip 31g 27mm Sideport 20PK (Green)
00883205022837NaviTip 31g 21mm Sideport 50PK (Yellow)
00883205022820NaviTip 31g 21mm Sideport 20PK (Yellow)

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