Pure Global

Fluid specimen concentration filter IVD - UK MHRA Medical Device Registration

Fluid specimen concentration filter IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 109897. The device is manufactured by Merck Millipore Ltd from Ireland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Millipore (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.

Free Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Fluid specimen concentration filter IVD
MHRA Device ID: 109897โ€ขRef: 109897

Device Type

In Vitro Diagnostic Device

Devices

Fluid specimen concentration filter IVD

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Sep 3, 2024

Manufacturer Information

Address

Tullagreen Carrigtwohill

Cork, Co. Cork, Ireland

Created Date

Aug 25, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

2 Fleming Road Kirkton Campus

Livingston, West Lothian, Scotland, United Kingdom

Postcode: EH54 7BN

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing