Ion-selective analyser IVD - UK MHRA Medical Device Registration

Ion-selective analyser IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180598. The device is manufactured by EXIAS Medical GmbH from Austria, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap 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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Ion-selective analyser IVD

MHRA Device ID: 180598•Ref: 180598

Device Type

In Vitro Diagnostic Device

Devices

Ion-selective analyser IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Sep 13, 2024

Manufacturer Information

Name

EXIAS Medical GmbH

Address

Kratkystraße 2 8020 Graz

-, Austria

Created Date

Oct 20, 2023

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Other Products from EXIAS Medical GmbH (2)

Multiple electrolyte IVD, control

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Multiple electrolyte IVD, kit, ion-selective electrode (ISE)

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Ion-selective analyser IVD - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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