Enterovirus antigen (serotypes 68-71) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Enterovirus antigen (serotypes 68-71) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 154257. The device is manufactured by Avioq Bio-tech 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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Enterovirus antigen (serotypes 68-71) IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 154257•Ref: 154257

Device Type

In Vitro Diagnostic Device

Devices

Enterovirus antigen (serotypes 68-71) IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Name

Avioq Bio-tech Co., Ltd.

Address

1 Kangyuan Avenue, Laishan District, Yantai

Shandong Province, China

Created Date

Aug 15, 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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Other Products from Avioq Bio-tech Co., Ltd. (1)

Monkeypox virus antigen IVD, kit, rapid ICT, clinical

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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Enterovirus antigen (serotypes 68-71) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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