Staphaurex Plus (450 test)

GUDID 05056080501529

REMEL EUROPE LIMITED

Staphylococcus aureus culture isolate antigen IVD, kit, agglutination
Primary Device ID05056080501529
NIH Device Record Key37fde97c-e94e-498f-84b0-61bec5591535
Commercial Distribution StatusIn Commercial Distribution
Brand NameStaphaurex Plus (450 test)
Version Model NumberR30950201
Company DUNS232600853
Company NameREMEL EUROPE LIMITED
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+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com
Phone+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com
Phone+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com
Phone+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com
Phone+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com
Phone+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com
Phone+4401256694238
Emailmicrobiology.techsupport.uk@thermofisher.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105056080501529 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWXKit, Screening, Staphylococcus Aureus

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-29
Device Publish Date2021-07-21

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