ADVANCED ECHO TECHNOLOGY
France FR-MF-000000599 Last updated 31 May 2026
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- Devices
- 4
- Registries
- EUDAMEDGUDID
- FDA recalls
- 0
Catalogue
Melody Ref PCI; MEL; PRW; ECI; CP5; FPB
Melody Patient Ref MEL; PCI; PRW
Melody Expert Virtual Ref FPB-MEV; MEV
Melody Expert Ref CP5; ECI; FPB
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.
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.
Information
- Country
- France
- Address
- 7, RUE CLOS HAUT DE LA BOUCHARDIE, NAVEIL, France
- Website
- www.adechotech.com/
- [email protected]
- Phone
- +33967174746
- PRRC contact
- Aafaf MAROUANI
- EUDAMED SRN
- FR-MF-000000599
- DUNS number
- 260110102