Serum amyloid A IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Serum amyloid A IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 170221. The device is manufactured by Guangzhou Wondfo Biotech Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Serum amyloid A IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 170221•Ref: 170221

Device Type

In Vitro Diagnostic Device

Devices

Serum amyloid A IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jul 31, 2024

Manufacturer Information

Name

Guangzhou Wondfo Biotech Co., Ltd.

Address

No.8 Lizhishan Road, Science City, Huangpu District

Guangzhou, China

Created Date

Mar 7, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Serum amyloid A IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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