Monkeypox virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Monkeypox virus antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163521. The device is manufactured by Shenzhen Watmind Medical Co., Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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In Vitro Diagnostic Device

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Monkeypox virus antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 163521•Ref: 163521

Device Type

In Vitro Diagnostic Device

Devices

Monkeypox virus antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 29, 2023

Manufacturer Information

Name

Shenzhen Watmind Medical Co., Ltd

Address

8th Floor, Building A, No.16-1, Jinhui Road, Jinsha Community, Kengzi Subdistrict, Pingshan District

Shenzhen, China

Created Date

Dec 20, 2022

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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Monkeypox virus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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