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Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 105725. The device is manufactured by BIOKIT S.A. from Spain, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Werfen Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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In Vitro Diagnostic Device
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Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry
MHRA Device ID: 105725โ€ขRef: 105725

Device Type

In Vitro Diagnostic Device

Devices

Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 21, 2024

Manufacturer Information

Address

Av. Can Montcau, 7 08186 Lliรงร  d'Amunt

Barcelona, Spain

Created Date

Aug 20, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

712 The Quadrant, Cavendish Avenue, Birchwood, Warrington WA3 6DE Manchester

Manchester, England, United Kingdom

Postcode: WA3 6DE

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