Ultrasound-guided intrauterine radio-frequency ablation system handpiece/electrode - UK MHRA Medical Device Registration
Ultrasound-guided intrauterine radio-frequency ablation system handpiece/electrode is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95137. The device is manufactured by Gynesonics Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Obelis UK Ltd.
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.
Device Type
General Medical Device
Devices
Ultrasound-guided intrauterine radio-frequency ablation system handpiece/electrode
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Aug 30, 2024
Name
Gynesonics Inc.Address
600 Chesapeake Drive
Reedwood City, CA, United States
Created Date
Aug 16, 2021
Name
Obelis UK LtdRelationship Type
Address
Sandford Gate, East Point Business Park
Oxford , England, United Kingdom
Postcode: OX4 6LB
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Ultrasound-guided intrauterine radio-frequency ablation system
Type: General Medical Device
Registered: Nov 26, 2024
Ultrasound-guided intrauterine radio-frequency ablation system handpiece/electrode
Type: General Medical Device
Registered: Nov 26, 2024
Ultrasound-guided intrauterine radio-frequency ablation system handpiece/electrode
Type: General Medical Device
Registered: Nov 26, 2024
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