Multiple febrile infection-associated bacteria antigen IVD, reagent - UK MHRA Medical Device Registration

Multiple febrile infection-associated bacteria antigen IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 201985. The device is manufactured by Chongqing iSIA BIO-Technology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CMC Medical Devices LTD.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Multiple febrile infection-associated bacteria antigen IVD, reagent

MHRA Device ID: 201985•Ref: 201985

Device Type

In Vitro Diagnostic Device

Devices

Multiple febrile infection-associated bacteria antigen IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 2, 2024

Manufacturer Information

Name

Chongqing iSIA BIO-Technology Co., Ltd.

Address

No. 388 Jingdongfang Avenue, Beibei District,

Chongqing,, China

Created Date

Sep 27, 2024

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Multiple febrile infection-associated bacteria antigen IVD, reagent - UK MHRA Medical Device Registration

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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