United Kingdom MHRA device registration 76223

Dual-chamber implantable defibrillator

United Kingdom flagUnited Kingdom·Active Implantable Device·Microport CRM S.r.l·Registered Nov 26, 2024
Registration details
Device ID
76223
MHRA Reference Number
76223
Date Registered
Nov 26, 2024
Last Updated
Feb 23, 2024
Device classification
Device Type
Active Implantable Device
Devices
Dual-chamber implantable defibrillator
Manufacturer
Address
Via Crescentino s.n. Via Crescentino s.n.
Saluggia, VC, Italy
Created Date
Mar 22, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Willow House, Sealand Road Park West
Chester, Cheshire, England, United Kingdom
Postcode: CH1 4RW
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About this record

Dual-chamber implantable defibrillator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 76223. The device is manufactured by Microport CRM S.r.l from Italy, classified as Active Implantable 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.

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