United Kingdom MHRA device registration 71666

Cardiac resynchronization therapy implantable defibrillator

United Kingdom·Active implantable device (Directive 90/385/EEC only)·Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation·Registered Apr 1, 2021

Registration details

Device ID: 71666
Date Registered: Apr 1, 2021
Last Updated: Dec 22, 2022

Device classification

Device Type: Active implantable device (Directive 90/385/EEC only)
Devices: Cardiac resynchronization therapy implantable defibrillator
Type: Active implantable Medical device

Manufacturer

Name: Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation
Address: 4100 Hamline Avenue North
St. Paul, Minnesota, United States
Created Date: Apr 1, 2021

Authorized Representative

Name: Boston Scientific Limited
Relationship Type: UK Responsible Person
Address: 100 New Bridge Street
London, England, United Kingdom
Postcode: EC4V 6JA

Similar products

Devices with a matching generic name or device type registered with MHRA

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: Active Implantable Device

Manufacturer: BIOTRONIK SE & Co. KG

Device ID: 73515

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: General Medical Device

Manufacturer: BIOTRONIK SE & Co. KG

Device ID: 171630

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: Active Implantable Device

Manufacturer: Microport CRM S.r.l

Device ID: 76224

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: General Medical Device

Manufacturer: Medtronic, Inc

Device ID: 163676

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: General Medical Device

Manufacturer: Microport CRM S.r.l

Device ID: 89480

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: Active Implantable Device

Manufacturer: Medtronic, Inc

Device ID: 70805

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: Active Implantable Device

Manufacturer: St. Jude Medical Cardiac Rhythm Management Division

Device ID: 66100

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: General Medical Device

Manufacturer: Abbott Medical

Device ID: 156509

Cardiac resynchronization therapy implantable defibrillatorNov 26, 2024

Type: Active Implantable Device

Manufacturer: Medtronic, Inc

Device ID: 67150

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead, wireless connectionApr 5, 2022

Type: Active implantable device (Directive 90/385/EEC only)

Manufacturer: Stimwave Technologies Incorporated

Device ID: 143463

Other products from Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation

Additional devices registered by the same manufacturer

Vascular guide-catheter, single-useMar 26, 2025

Type: General Medical Device

Device ID: 214186

Pacing/defibrillation lead repair kitFeb 5, 2025

Type: General Medical Device

Device ID: 210140

Cardiac/peripheral vascular guidewire, single-useJan 24, 2025

Type: General Medical Device

Device ID: 209434

Pacing lead implantation adaptorJan 24, 2025

Type: General Medical Device

Device ID: 209433

Implantable electrical stimulation lead suture sleeveJan 24, 2025

Type: General Medical Device

Device ID: 209432

Endocardial/interventricular septal pacing leadDec 21, 2024

Type: General Medical Device

Device ID: 183486

Endocardial/interventricular septal pacing leadDec 21, 2024

Type: General Medical Device

Device ID: 183485

Endocardial/interventricular septal pacing leadDec 21, 2024

Type: General Medical Device

Device ID: 200941

Implantable cardiac device management application softwareOct 24, 2024

Type: System or Procedure Pack

Device ID: 203703

Pacing/defibrillation lead repair kitSep 14, 2024

Type: General Medical Device

Device ID: 200940

Other products from same authorized representative

Additional devices represented by Boston Scientific Limited in the UK

Implantable electrical stimulation device management softwareNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 202924

Percutaneous radio-frequency ablation probe, denervation, bipolarNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 205622

Deep brain electrical stimulation systemNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 200044

Deep brain electrical stimulation systemNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 200395

Percutaneous radio-frequency ablation probe cannula, single-useNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 205616

Percutaneous radio-frequency ablation probe cannula, single-useNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 205624

Deep brain electrical stimulation systemNov 26, 2024

Type: Active Implantable Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 178257

Deep brain electrical stimulation systemNov 26, 2024

Type: Active Implantable Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 178259

Deep brain electrical stimulation systemNov 26, 2024

Type: Active Implantable Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 71599

Percutaneous radio-frequency ablation probe, denervation, bipolarNov 26, 2024

Type: General Medical Device

Manufacturer: Boston Scientific Neuromodulation Corporation

Device ID: 205623

About this record

Cardiac resynchronization therapy implantable defibrillator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 71666. The device is manufactured by Cardiac Pacemakers, Inc., a subsidiary of Boston Scientific Corporation from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Boston Scientific Limited.

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.

Free DatabasePowered by Pure Global AIMHRA RegisteredActive implantable device (Directive 90/385/EEC only)