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Home > Our scientific expertise > Registration of diagnostic kits > The register of diagnostic kits

Register of diagnostic kits certified by the OIE as validated as fit for purpose

'Fit for purpose' means that the kit has to be validated to such a level to show that the kit's results can be interpreted to have a defined meaning in terms of diagnosis or another biological property being examined.

Disease

Name of the
Diagnostic kit

Name of the Manufacturer

Contact

Type of kit

Purpose(s) validated

Date and Number of registration

Validation studies Abstract Sheet

Kit insert

Avian Influenza

BioChek Avian Influenza Antibody test kit

BioChek UK Ltd

info@biochek.com

ELISA


see Resolution No XXVII adopted in May 2008 by the World Assembly of the OIE Delegates

May 2008
Registration Number: 20080203


AS Biochek AI Antibody test kit

User's manual

White spot disease

IQ 2000TM WSSV Detection and Prevention System

GeneReach Biotechnology Corp

sales@ genereach .com

PCR


see Resolution No XXVII adopted in May 2008 by the World Assembly of the OIE Delegates

May 2008
Registration Number: 20080304


AS IQ 2000

User's manual

Bovine spongiform encephalopathy

Prionics AG - Check Western

Prionics AG

info@prionics.com

Western Blot


see Resolution No XXVII adopted in May 2008 by the World Assembly of the OIE Delegates

May 2008
Registration Number: 20080102


AS Prionics AG-Check WESTERN

User's manual

Transmissible Spongiform Encephalopathies

TeSeETM Western Blot

Bio-Rad

tse@bio-rad.com

Western Blot


see Resolution No XXVI adopted in May 2009 by the World Assembly of the OIE Delegates

May 2009 Registration Number: 20090105


AS TeSeE WB

User's manual

Salmonellosis

Check&Trace Salmonella

Check-Points B.V.

serovar@check-points.com for technical questions

 

info@check-points.com for general questions

Multiplex LDR PCR reaction followed by detection on a diagnostic micro array


see Resolution No 24 adopted in May 2011 by the World Assembly of the OIE Delegates

May 2011
Registration Number: 20110106


AS CTS

User's manual

Bovine tuberculosis

Mycobacterium bovis Antibody Test Kit

IDEXX Laboratories

lpdtechservices.com

Indirect ELISA


see Resolution No 24 adopted in May 2012 by the World Assembly of the OIE Delegates

May 2012
Registration Number: 20120107


AS MBAT

User's manual

Contact OIESVCRDA

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