PIVOT Non-Latex Disposable Prophy Angle NL Firm Cup Box 144 1100053

GUDID D02411000533

PIVOT Non-Latex Disposable Prophy Angle NL Firm Cup Box of 144 single use prophy angles for dental prophylaxis procedures

Preventech

Dental polishing cup, single-use
Primary Device IDD02411000533
NIH Device Record Keyc549a92b-1039-4c05-a8e4-dcba54f9ad6d
Commercial Distribution StatusIn Commercial Distribution
Brand NamePIVOT Non-Latex Disposable Prophy Angle NL Firm Cup Box 144
Version Model Number1100053
Catalog Number1100053
Company DUNS090735093
Company NamePreventech
Device Count144
DM Exemptfalse
Pre-market Exemptfalse
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com
Phone7048492416
Emailcustomerservice@preventech.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD0241100053 [Primary]
HIBCCD02411000533 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EHKCup, Prophylaxis

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-21
Device Publish Date2023-06-13

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