United Kingdom MHRA device registration 166038

Clinical laboratory information system application software

United Kingdom·In Vitro Diagnostic Device·Beckman Coulter Biomedical GmbH·Registered Nov 26, 2024

Registration details

Device ID: 166038
MHRA Reference Number: 166038
Date Registered: Nov 26, 2024
Last Updated: Nov 19, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Clinical laboratory information system application software
Type: Class A

Manufacturer

Name: Beckman Coulter Biomedical GmbH
Address: Sauerbruchstr. 50
Munich, Germany
Created Date: Dec 21, 2021

Authorized Representative

Name: Beckman Coulter UK Ltd
Relationship Type: UK Responsible Person
Address: Oakley Court Kingsmead Busines sPark London Rd
High Wycombe, Bucks, United Kingdom
Postcode: HP11 1JU

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About this record

Clinical laboratory information system application software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 166038. The device is manufactured by Beckman Coulter Biomedical GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Beckman Coulter 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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