Pure Global

Faecal specimen collection kit IVD, home-use - UK MHRA Medical Device Registration

Faecal specimen collection kit IVD, home-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 169731. The device is manufactured by GP Medical Devices A/S from Denmark, 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.

Free Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Faecal specimen collection kit IVD, home-use
MHRA Device ID: 169731โ€ขRef: 169731

Device Type

In Vitro Diagnostic Device

Devices

Faecal specimen collection kit IVD, home-use

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

Address

Nupark 51

Holstebro, Denmark

Created Date

Mar 30, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing