Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 166666. The device is manufactured by Xiamen Wiz 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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Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical

MHRA Device ID: 166666•Ref: 166666

Device Type

In Vitro Diagnostic Device

Devices

Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 19, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

Xiamen Wiz Biotech Co., Ltd.

Address

3-4 Floor, No. A16 Building, Bio-medical Workshop, 2030 Wengjiao Xi Road, Haicang District, 361026

Xiamen, Fujian Province, China

Created Date

Dec 15, 2022

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

MedTech Regulatory Expert

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Mycoplasma pneumoniae immunoglobulin M (IgM) antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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