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Legionella pneumophila antigen IVD, control - UK MHRA Medical Device Registration

Legionella pneumophila antigen IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195136. 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.

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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Legionella pneumophila antigen IVD, control
MHRA Device ID: 195136Ref: 195136

Device Type

In Vitro Diagnostic Device

Devices

Legionella pneumophila antigen IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Address

Crealys Science Park Rue Guillaume Fouquet 11

Gembloux, Namur, Belgium

Created Date

Jun 11, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

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