Angiotensin converting enzyme (ACE) IVD, reagent - UK MHRA Medical Device Registration
Angiotensin converting enzyme (ACE) IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85105. The device is manufactured by Trinity Biotech Plc from Ireland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is IVDeology UKRP 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.
Device Type
In Vitro Diagnostic Device
Devices
Angiotensin converting enzyme (ACE) IVD, reagent
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Apr 10, 2024
Address
IDA Business Park Southern Cross Road
Bray, Co. Wicklow, Ireland
Created Date
Jun 11, 2021
Relationship Type
Address
Maidstone Innovation Centre Gidds Pond Way
Maidstone, Kent, England, United Kingdom
Postcode: ME14 5FY
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