NEXT Medium Spearmint Prophy Paste Box 200 220293

GUDID D0242202933

NEXT Medium Spearmint Prophy Paste Box of 200 2.0g prophy cup units for dental prophylaxis procedures

Preventech

Dentifrice
Primary Device IDD0242202933
NIH Device Record Key420587ff-2cf4-4967-aa71-2fda296d5d40
Commercial Distribution StatusIn Commercial Distribution
Brand NameNEXT Medium Spearmint Prophy Paste Box 200
Version Model Number220293
Catalog Number220293
Company DUNS090735093
Company NamePreventech
Device Count200
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 Datefalse
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
HIBCCD024220293 [Primary]
HIBCCD0242202933 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EJRAgent, Polishing, Abrasive, Oral Cavity

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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