Promolux Polymer pink veined 1025023

GUDID D7091025023

Promolux Polymer pink veined, 1000g

Merz Dental GmbH

Dental appliance fabrication material, resin
Primary Device IDD7091025023
NIH Device Record Key8bac33a7-95ad-442a-838c-f6beda46839f
Commercial Distribution StatusIn Commercial Distribution
Brand NamePromolux Polymer pink veined
Version Model NumberPromolux Polymer pink veined, 1000g
Catalog Number1025023
Company DUNS324914910
Company NameMerz Dental 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 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

Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de
Phone+494381403411
Emailclaudia.bobrowski@merz-dental.de

Device Dimensions

Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram
Weight1000 Gram

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD7091025023 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

EBIResin, Denture, Relining, Repairing, Rebasing

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2021-11-10
Device Publish Date2020-06-10

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