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 148258. 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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Blood test-based differential diagnosis interpretive software IVD

MHRA Device ID: 148258•Ref: 148258

Device Type

In Vitro Diagnostic Device

Devices

Blood test-based differential diagnosis interpretive software IVD

Type

IVD General

Date Registered

May 24, 2022

Last Updated

Aug 15, 2023

Manufacturer Information

Name

Janssen Pharmaceutica NV

Address

Turnhoutseweg 30

Beerse, 2340 Beerse, Belgium

Created Date

May 24, 2022

Authorized Representative

Name

Johnson & Johnson Medical Ltd

Relationship Type

UK Responsible Person

Address

Baird House 4 Lower Gilmore Bank

Edinburgh, Scotland, United Kingdom

Postcode: EH3 9QP

DJ Fang

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Other Products from Janssen Pharmaceutica NV (1)

Blood test-based differential diagnosis interpretive software IVD

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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

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