Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 165365. The device is manufactured by BIOSYNEX SA from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 165365•Ref: 165365

Device Type

In Vitro Diagnostic Device

Devices

Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

BIOSYNEX SA

Address

22 Boulevard Sebastien Brant ILLKIRCH-GRAFFENSTADEN

Strasbourg, Bas-Rhin, France

Created Date

Jun 24, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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