General specimen collection kit IVD, clinical - UK MHRA Medical Device Registration

General specimen collection kit IVD, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 167516. The device is manufactured by Agendia N.V. from Netherlands, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group UK, 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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General specimen collection kit IVD, clinical

MHRA Device ID: 167516•Ref: 167516

Device Type

In Vitro Diagnostic Device

Devices

General specimen collection kit IVD, clinical

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Agendia N.V.

Address

Radarweg 60

Amsterdam, Netherlands

Created Date

May 11, 2022

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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Other Products from Agendia N.V. (1)

General specimen collection kit IVD, clinical

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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General specimen collection kit IVD, clinical - UK MHRA Medical Device Registration

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