Cystic fibrosis IVD, control - UK MHRA Medical Device Registration

Cystic fibrosis IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 155890. The device is manufactured by Quantimetrix Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP 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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Cystic fibrosis IVD, control

MHRA Device ID: 155890•Ref: 155890

Device Type

In Vitro Diagnostic Device

Devices

Cystic fibrosis IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 10, 2023

Manufacturer Information

Name

Quantimetrix Corporation

Address

2005 Manhattan Beach Blvd.

Redondo Beach , California, United States

Created Date

Dec 30, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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Other Products from Quantimetrix Corporation (5)

Other Products from Same Authorized Representative (10)

Cystic fibrosis IVD, control - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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