United Kingdom MHRA device registration 72675

Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator

United Kingdom·Active implantable device (Directive 90/385/EEC only)·St. Jude Medical·Registered Apr 6, 2021

Registration details

Device ID: 72675
Date Registered: Apr 6, 2021
Last Updated: Dec 22, 2022

Device classification

Device Type: Active implantable device (Directive 90/385/EEC only)
Devices: Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
Type: Active implantable Medical device

Manufacturer

Name: St. Jude Medical
Address: 6901 Preston Road
Plano, Texas, United States
Created Date: Apr 6, 2021

Authorized Representative

Name: Abbott Medical UK Limited
Relationship Type: UK Responsible Person
Address: Elder House Central Boulevard Blythe Valley Business Park
Solihull, West Midlands, England, United Kingdom
Postcode: B90 8AJ

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About this record

Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 72675. The device is manufactured by St. Jude Medical from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is Abbott Medical UK 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.

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