Buffered sample diluent IVD - UK MHRA Medical Device Registration

Buffered sample diluent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203923. The device is manufactured by HYPHEN BioMed from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Sysmex 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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Buffered sample diluent IVD

MHRA Device ID: 203923•Ref: 203923

Device Type

In Vitro Diagnostic Device

Devices

Buffered sample diluent IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 17, 2024

Manufacturer Information

Name

HYPHEN BioMed

Address

155 rue d'Eragny

Neuville-Sur-Oise, France

Created Date

Jan 31, 2023

Authorized Representative

Name

Sysmex UK Ltd

Relationship Type

UK Responsible Person

Address

Sysmex House Garamonde Drive Wymbush

Milton Keynes, Buckinghamshire, England, United Kingdom

Postcode: MK8 8DF

DJ Fang

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Other Products from HYPHEN BioMed (10)

Other Products from Same Authorized Representative (10)

Buffered sample diluent IVD - UK MHRA Medical Device Registration

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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