Pure Global

Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Trichomonas vaginalis 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 194955. The device is manufactured by Bifour Biotech Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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.

Free Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinical
MHRA Device ID: 194955โ€ขRef: 194955

Device Type

In Vitro Diagnostic Device

Devices

Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

May 31, 2024

Manufacturer Information

Address

4677 Old Ironsides Drive, Suite 300,Santa Clara

California, United States

Created Date

May 24, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing