Chlamydia trachomatis antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Chlamydia trachomatis 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 97103. The device is manufactured by Zhejiang Orient Gene Biotech Co. Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SENSUS Group 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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In Vitro Diagnostic Device

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Chlamydia trachomatis antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 97103•Ref: 97103

Device Type

In Vitro Diagnostic Device

Devices

Chlamydia trachomatis antigen IVD, kit, rapid ICT, clinical

Type

IVD Annex II List B

Date Registered

Nov 26, 2024

Last Updated

Jul 25, 2024

Manufacturer Information

Name

Zhejiang Orient Gene Biotech Co. Ltd

Address

3787#, East Yangguang Avenue, Dipu Street Anji, Huzhou

Zhejiang, China

Created Date

Aug 20, 2021

Authorized Representative

Name

SENSUS Group Ltd

Relationship Type

UK Responsible Person

Address

The Barn Tednambury Farm Tednambury

Spellbrook, Hertfordshire, England, United Kingdom

Postcode: CM23 4BD

DJ Fang

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Other Products from Zhejiang Orient Gene Biotech Co. Ltd (10)

Other Products from Same Authorized Representative (10)

Chlamydia trachomatis antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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