Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use - UK MHRA Medical Device Registration
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 77938. 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.
Device Type
General Medical Device
Devices
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
Apr 30, 2024
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable
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Registered: Nov 26, 2024
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