Dual-chamber implantable defibrillator - UK MHRA Medical Device Registration
Dual-chamber implantable defibrillator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89479. The device is manufactured by Microport CRM S.r.l from Italy, classified as General Medical Device. The authorized representative in the UK is MicroPort CRM 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
General Medical Device
Devices
Dual-chamber implantable defibrillator
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Feb 23, 2024
Address
Via Crescentino s.n. Via Crescentino s.n.
Saluggia, VC, Italy
Created Date
Mar 22, 2021
Relationship Type
Address
Willow House, Sealand Road Park West
Chester, Cheshire, England, United Kingdom
Postcode: CH1 4RW
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