Percutaneous radio-frequency ablation probe cannula, single-use - UK MHRA Medical Device Registration

Percutaneous radio-frequency ablation probe cannula, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 77937. The device is manufactured by DIROS TECHNOLOGY INC from Canada, 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 cannula, single-use

MHRA Device ID: 77937•Ref: 77937

Device Type

General Medical Device

Devices

Percutaneous radio-frequency ablation probe cannula, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Apr 30, 2024

Manufacturer Information

Name

DIROS TECHNOLOGY INC

Address

120 Gibson Drive

Markham, Ontario, Canada

Created Date

Apr 29, 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 DIROS TECHNOLOGY INC (10)

Other Products from Same Authorized Representative (10)

Percutaneous radio-frequency ablation probe cannula, single-use - 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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