Endocardial defibrillation lead
- Device ID
- 153915
- MHRA Reference Number
- 153915
- Date Registered
- Nov 26, 2024
- Last Updated
- Feb 23, 2024
- Device Type
- General Medical Device
- Devices
- Endocardial defibrillation lead
- Type
- Class III
- Address
- Via Crescentino s.n. Via Crescentino s.n.Saluggia, VC, Italy
- Created Date
- Mar 22, 2021
- Relationship Type
- UK Responsible Person
- Address
- Willow House, Sealand Road Park West Chester, Cheshire, England, United KingdomPostcode: CH1 4RW
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by MicroPort CRM Ltd in the UK
Endocardial defibrillation lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 153915. 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.