Human genomic analysis interpretive software - UK MHRA Medical Device Registration

Human genomic analysis interpretive software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95026. The device is manufactured by Roche Sequencing Solutions, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Roche Diagnostics Limited.

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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Human genomic analysis interpretive software

MHRA Device ID: 95026•Ref: 95026

Device Type

In Vitro Diagnostic Device

Devices

Human genomic analysis interpretive software

Type

IVD Annex II List B

Date Registered

Sep 1, 2024

Last Updated

Jul 10, 2024

Manufacturer Information

Name

Roche Sequencing Solutions, Inc.

Address

4300 Hacienda Dr.

Pleasanton, United States

Created Date

Aug 16, 2021

Authorized Representative

Name

Roche Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Roche Diagnostics Limited Charles Avenue

Burgess Hill, West Sussex, United Kingdom

Postcode: RH15 9RY

DJ Fang

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Human genomic analysis interpretive software - UK MHRA Medical Device Registration

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