United Kingdom MHRA device registration 179095

Blood test-based differential diagnosis interpretive software IVD

United Kingdom·In Vitro Diagnostic Device·Janssen Pharmaceutica NV·Registered Nov 26, 2024

Registration details

Device ID: 179095
MHRA Reference Number: 179095
Date Registered: Nov 26, 2024
Last Updated: Jun 29, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Blood test-based differential diagnosis interpretive software IVD
Type: IVD General

Manufacturer

Name: Janssen Pharmaceutica NV
Address: Turnhoutseweg 30 2340 Beerse
Beerse, Belgium
Created Date: Sep 15, 2023

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

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Additional devices registered by the same manufacturer

Blood test-based differential diagnosis interpretive software IVDMay 24, 2022

Type: In Vitro Diagnostic Device

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About this record

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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