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

Faecal specimen collection kit IVD, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 130954. The device is manufactured by ORGENTEC Diagnostika GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK 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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Faecal specimen collection kit IVD, clinical
MHRA Device ID: 130954โ€ขRef: 130954

Device Type

In Vitro Diagnostic Device

Devices

Faecal specimen collection kit IVD, clinical

Type

IVD General

Date Registered

Aug 10, 2021

Last Updated

Oct 12, 2023

Manufacturer Information

Address

Carl-Zeiss-Str. 49-51

Mainz, Rheinhessen-Pfalz, Germany

Created Date

Aug 10, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

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