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Blood test-based differential diagnosis interpretive software IVD - UK MHRA Medical Device Registration

Blood test-based differential diagnosis interpretive software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 179095. The device is manufactured by Janssen Pharmaceutica NV from Belgium, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Johnson & Johnson Medical 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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In Vitro Diagnostic Device
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Blood test-based differential diagnosis interpretive software IVD
MHRA Device ID: 179095โ€ขRef: 179095

Device Type

In Vitro Diagnostic Device

Devices

Blood test-based differential diagnosis interpretive software IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 29, 2024

Manufacturer Information

Address

Turnhoutseweg 30 2340 Beerse

Beerse, Belgium

Created Date

Sep 15, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

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