Pure Global

Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator - UK MHRA Medical Device Registration

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 195696. The device is manufactured by Nevro Corporation from United States, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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 Database
Powered by Pure Global AI
MHRA Registered
General Medical Device
๐Ÿ‡ฌ๐Ÿ‡ง
Trial spinal cord/peripheral nerve percutaneous analgesic electrical stimulation system pulse generator
MHRA Device ID: 195696

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Jun 22, 2024

Manufacturer Information

Address

1800 Bridge Parkway

Redwood City, CA, United States

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing