United Kingdom MHRA device registration 205961

Transcutaneous electrical stimulation lead

United Kingdom flagUnited Kingdom·General Medical Device·Medtronic Xomed Inc·Registered Nov 28, 2024DREGIY
Registration details
Device ID
205961
Status
DREGIY
Date Registered
Nov 28, 2024
Device classification
Device Type
General Medical Device
Type
Class I
Manufacturer
Address
6743 Southport Drive North
Jacksonville, FL, United States
Similar products

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

Other products from Medtronic Xomed Inc

Additional devices registered by the same manufacturer

About this record

Transcutaneous electrical stimulation lead is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205961. The device is manufactured by Medtronic Xomed Inc 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 DatabasePowered by Pure Global AIMHRA RegisteredGeneral Medical Device