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Faecal specimen container IVD, DNA preservation solution - UK MHRA Medical Device Registration

Faecal specimen container IVD, DNA preservation solution is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 122433. The device is manufactured by DNA Genotek Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) 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.

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In Vitro Diagnostic Device
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Faecal specimen container IVD, DNA preservation solution
MHRA Device ID: 122433โ€ขRef: 122433

Device Type

In Vitro Diagnostic Device

Devices

Faecal specimen container IVD, DNA preservation solution

Type

IVD General

Date Registered

Jun 24, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Address

3000 - 500 Palladium Drive

Ottawa, Ontario, Canada

Created Date

Nov 23, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 โ€“ UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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