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 203181. 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.

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Ultrasound-guided intrauterine radio-frequency ablation system handpiece/electrode

MHRA Device ID: 203181•Ref: 203181

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

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

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