Ultrasound-guided intrauterine radio-frequency ablation system - UK MHRA Medical Device Registration

Ultrasound-guided intrauterine radio-frequency ablation system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203182. 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.

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Ultrasound-guided intrauterine radio-frequency ablation system

MHRA Device ID: 203182•Ref: 203182

Device Type

General Medical Device

Devices

Ultrasound-guided intrauterine radio-frequency ablation system

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Aug 30, 2024

Manufacturer Information

Name

Gynesonics Inc.

Address

600 Chesapeake Drive

Reedwood City, CA, United States

Created Date

Aug 16, 2021

Authorized Representative

Name

Obelis UK Ltd

Relationship Type

UK Responsible Person

Address

Sandford Gate, East Point Business Park

Oxford , England, United Kingdom

Postcode: OX4 6LB

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Other Products from Gynesonics Inc. (10)

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Ultrasound-guided intrauterine radio-frequency ablation system - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Ultrasound-guided intrauterine radio-frequency ablation system

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Ultrasound-guided intrauterine radio-frequency ablation system intrauterine ultrasound transducer, single-use

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