Qu-resin pink 54001161

GUDID EBRE540011619

Qu-resin pink 1 Assortment

bredent GmbH & Co. KG

Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin Dental composite resin
Primary Device IDEBRE540011619
NIH Device Record Key77a8f95e-e1ea-4664-a0cd-061d7bf8323d
Commercial Distribution StatusIn Commercial Distribution
Brand NameQu-resin pink
Version Model Number54001161
Catalog Number54001161
Company DUNS341086190
Company Namebredent GmbH & Co. KG
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com
Phone+4907309872451
Emailinfo@bredent.com

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight
Special Storage Condition, SpecifyBetween 0 and 0 *keep out of sunlight

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEBRE540011610 [Primary]
HIBCCEBRE540011619 [Package]
Contains: EBRE540011610
Package: dummy [1 Units]
Discontinued: 2023-09-07
Not in Commercial Distribution

FDA Product Code

EKODenture preformed (partially prefabricated denture)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-09-15
Device Publish Date2023-09-07

On-Brand Devices [Qu-resin pink]

EBRE540011659Qu-resin pink 50 ml
EBRE540011619Qu-resin pink 1 Assortment

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