Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar - UK MHRA Medical Device Registration

Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 101594. The device is manufactured by STARmed CO LTD from South Korea, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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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Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar

MHRA Device ID: 101594•Ref: 101594

Device Type

General Medical Device

Devices

Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar

Type

Class IIb

Date Registered

Jul 8, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

STARmed CO LTD

Address

158 Haneulmaeul-ro Ilsandong-gu

Gyeonggi-do, Goyang-si, South Korea

Created Date

Aug 31, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Other Products from STARmed CO LTD (10)

Other Products from Same Authorized Representative (10)

Percutaneous radio-frequency ablation probe, tumour-ablation, bipolar - 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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