Proteus OXK Agglutinating Serum

GUDID 05056080501611

REMEL EUROPE LIMITED

Multiple Rickettsia species (spotted fever group) total antibody IVD, control
Primary Device ID05056080501611
NIH Device Record Key62f0a181-4dbd-4b5a-a948-4feb8843e17a
Commercial Distribution StatusIn Commercial Distribution
Brand NameProteus OXK Agglutinating Serum
Version Model NumberR30165901
Company DUNS232600853
Company NameREMEL EUROPE LIMITED
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 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
GS105056080501611 [Primary]

FDA Product Code

GSYAntisera, Fluorescent, All Globulins, Proteus Spp.

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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05056080501253 - PathoDx Strep B Grouping Latex2021-07-29
05056080501260 - PathoDx Strep C Grouping Latex2021-07-29
05056080501277 - PathoDx Strep F Grouping Latex2021-07-29
05056080501284 - PathoDx Strep G Grouping Latex2021-07-29

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