United Kingdom MHRA device registration 86041

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension

United Kingdom·Active implantable device (Directive 90/385/EEC only)·Nevro Corporation·Registered Jun 22, 2021

Registration details

Device ID: 86041
Date Registered: Jun 22, 2021
Last Updated: Dec 22, 2022

Device classification

Device Type: Active implantable device (Directive 90/385/EEC only)
Devices: Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension
Type: Active implantable Medical device

Manufacturer

Name: Nevro Corporation
Address: 1800 Bridge Parkway
Redwood City, CA, United States
Created Date: Jun 22, 2021

Authorized Representative

Name: MDSS-UK RP LIMITED
Relationship Type: UK Responsible Person
Address: 6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP

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About this record

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 86041. The device is manufactured by Nevro Corporation from United States, classified as Active implantable device (Directive 90/385/EEC only). The authorized representative in the UK is MDSS-UK RP 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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