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AMINOGRAM

France FR-MF-000000671 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

About

Aminogram has been innovating for over 20 years to advance the science of body composition. Medical bioimpedance solutions for clinical analysis.

Translated from the manufacturer's own website. Source

What AMINOGRAM makes

Aminogram manufactures the Biody XPERTZM 3, a medical bioimpedance device designed for clinical assessment of body composition. This device measures impedance through the body to evaluate parameters such as fat mass, lean tissue, and hydration status, supporting diagnostic and monitoring applications in healthcare settings.

The Biody XPERTZM 3 is classified as a Class IIa medical device and is registered in the EU’s eudamed database. The company is based in France.

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 Aminogram manufacture?

Aminogram specializes in medical bioimpedance devices. Specifically, it produces the Biody XPERTZM 3, a device designed for clinical analysis of body composition. This includes measuring parameters like fat mass, lean tissue, and hydration status using bioimpedance technology, which helps healthcare professionals assess patient health in diagnostic and monitoring contexts.

Where is Aminogram based, and what is its primary focus?

Aminogram is based in France. The company focuses on advancing the science of body composition through medical bioimpedance solutions, aiming to provide clinically relevant insights for healthcare providers. Its primary product, the Biody XPERTZM 3, is tailored for precise, non-invasive body composition analysis in medical settings.

Which regulatory registries list Aminogram’s devices?

Aminogram’s devices are listed in the EU’s eudamed database, which is the official registry for medical devices within the European Union. This registration ensures transparency and compliance with EU medical device regulations, though it does not imply approval—only that the device is accounted for in the system.

How are Aminogram’s medical devices classified?

The Biody XPERTZM 3, Aminogram’s primary device, is classified as a Class IIa medical device. This classification is determined by its intended use and associated risk level, with Class IIa devices requiring compliance with specific EU regulations to ensure safety and performance, such as conforming to relevant harmonized standards and undergoing rigorous design controls.

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

Information

Country
France
Address
96, VC VOIE ATLAS , LA CIOTAT, France
Phone
+33442726603
PRRC contact
Cyrille MICHAUD
EUDAMED SRN
FR-MF-000000671