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Buffered sample diluent IVD - UK MHRA Medical Device Registration

Buffered sample diluent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180111. The device is manufactured by Randox Laboratories Limited from Northern Ireland, United Kingdom, classified as In Vitro Diagnostic Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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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Buffered sample diluent IVD
MHRA Device ID: 180111โ€ขRef: 180111

Device Type

In Vitro Diagnostic Device

Devices

Buffered sample diluent IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Sep 28, 2024

Manufacturer Information

Address

Ardmore 55 The Diamond Road

Crumlin, County Antrim, Northern Ireland, United Kingdom

Created Date

Nov 17, 2017

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