PROPHYflex 3 2018 violet 3 2018 violet

GUDID EKAV100699260

This is a medical device.

Kaltenbach & Voigt GmbH

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Primary Device IDEKAV100699260
NIH Device Record Keyd6068af9-6d2e-4c4e-9270-0df41f4918b5
Commercial Distribution StatusIn Commercial Distribution
Brand NamePROPHYflex 3 2018 violet
Version Model Number1.006.9926
Catalog Number3 2018 violet
Company DUNS332864359
Company NameKaltenbach & Voigt GmbH
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com
Phone+18475506800
Emailcustomerservice@kavo.com

Operating and Storage Conditions

Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius
Handling Environment TemperatureBetween -20 Degrees Celsius and 60 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEKAV100699260 [Primary]

FDA Product Code

EJRAGENT, POLISHING, ABRASIVE, ORAL CAVITY

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-22
Device Publish Date2016-09-26

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EKAV100765500 - Prophylaxe Set 2008L/2018 violett2021-03-09
EKAV100957450 - SMART LUX Case 619460L2021-03-09
EKAV100957460 - SMART Case 619460C2021-03-09
EKAV100957640 - PROPHYflex Perio Powder 20gr.2021-03-09
EKAV100960480 - EXPERT LUX Case 680465LRN2021-03-09

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