Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system - UK MHRA Medical Device Registration

Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 182392. The device is manufactured by Dornier MedTech GmbH from Germany, 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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Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system

MHRA Device ID: 182392•Ref: 182392

Device Type

General Medical Device

Devices

Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Dornier MedTech GmbH

Address

Argelsrieder Feld 7

Weßling, Bavarian, Germany

Created Date

Dec 20, 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

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Electromechanical orthopaedic extracorporeal shock wave/pneumatic pressure wave therapy system - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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