Legionella pneumophila antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Legionella pneumophila 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 195135. The device is manufactured by Coris Bioconcept Srl from Belgium, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 195135•Ref: 195135

Device Type

In Vitro Diagnostic Device

Devices

Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Name

Coris Bioconcept Srl

Address

Crealys Science Park Rue Guillaume Fouquet 11

Gembloux, Namur, Belgium

Created Date

Jun 11, 2024

Authorized Representative

Name

Launch Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

DJ Fang

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Legionella pneumophila antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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