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 100870. The device is manufactured by BGI Europe A/S from Denmark, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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Human genomic analysis interpretive software

MHRA Device ID: 100870•Ref: 100870

Device Type

In Vitro Diagnostic Device

Devices

Human genomic analysis interpretive software

Type

IVD Annex II List B

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Name

BGI Europe A/S

Address

Symfonivej 34

Herlev, Denmark

Created Date

Aug 30, 2021

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Other Products from BGI Europe A/S (10)

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Human genomic analysis interpretive software - UK MHRA Medical Device Registration

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Last Updated

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Created Date

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Address

DJ Fang

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