Ropak UV powder 52000165

GUDID EBRE520001659

Ropak UV powder 10 g

bredent GmbH & Co. KG

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Primary Device IDEBRE520001659
NIH Device Record Key66ce336d-f3ba-47c7-bfd6-298a9c52a716
Commercial Distribution StatusIn Commercial Distribution
Brand NameRopak UV powder
Version Model Number52000165
Catalog Number52000165
Company DUNS341086190
Company Namebredent GmbH & Co. KG
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
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

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCEBRE520001650 [Primary]
HIBCCEBRE520001659 [Package]
Contains: EBRE520001650
Package: dummy [1 Units]
Discontinued: 2016-09-20
Not in Commercial Distribution

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 Number3
Public Version Date2018-07-06
Device Publish Date2016-09-20

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