Human infectome analysis interpretive software IVD - UK MHRA Medical Device Registration

Human infectome analysis interpretive software IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 139559. 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 infectome analysis interpretive software IVD

MHRA Device ID: 139559•Ref: 139559

Device Type

In Vitro Diagnostic Device

Devices

Human infectome analysis interpretive software IVD

Type

IVD General

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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Human infectome analysis interpretive software IVD - UK MHRA Medical Device Registration

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Created Date

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DJ Fang

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