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ADVANCED ECHO TECHNOLOGY

France FR-MF-000000599 Last updated 31 May 2026

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Devices
4
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue4

What ADVANCED ECHO TECHNOLOGY makes

Advanced Echo Technology manufactures ultrasound-based virtual reality training platforms, including standalone systems (MELODY) and expert-level virtual simulators (MELODY EXPERT and MELODY EXPERT VIRTUAL) designed for medical professionals. These devices replicate clinical ultrasound scenarios for procedural training and skill assessment, supporting hands-on practice in a controlled digital environment.

The company’s portfolio is classified under EU Device Class IIa and is registered in the EUDAMED database. The manufacturer is based in France and adheres to EU regulatory requirements for medical simulation devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Advanced Echo Technology manufacture?

Advanced Echo Technology specialises in ultrasound-based virtual reality training platforms. These include standalone systems like the MELODY, as well as advanced virtual simulators such as the MELODY EXPERT and MELODY EXPERT VIRTUAL. These devices are designed to replicate clinical ultrasound scenarios, enabling medical professionals to practice and refine procedural skills in a controlled digital environment.

Where is Advanced Echo Technology based?

The company is headquartered in France, adhering to local regulatory standards and EU requirements for medical simulation devices.

Which regulatory registries list Advanced Echo Technology’s devices?

Advanced Echo Technology’s devices are registered in the EUDAMED database, which is the official European Union database for medical devices. This registry ensures transparency and compliance with EU regulatory frameworks.

How are Advanced Echo Technology’s devices classified under EU regulations?

The company’s devices fall under EU Device Class IIa, which is the second-lowest risk classification for medical devices. This classification is determined based on factors such as the intended use, potential risks, and the level of intervention involved in the device’s application.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
France
Address
7, RUE CLOS HAUT DE LA BOUCHARDIE, NAVEIL, France
Phone
+33967174746
PRRC contact
Aafaf MAROUANI
EUDAMED SRN
FR-MF-000000599
DUNS number
260110102