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Laboratoires I2M

France FR-MF-000000296 Last updated 21 Oct 2026

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Devices
5
Registries
EUDAMED
FDA recalls
0

Catalogue5

About

Treatment of excessive sweating of hands, sweating of feet and armpits (Hyperhidrose).

Translated from the manufacturer's own website. Source

What Laboratoires I2M makes

Laboratoires I2M manufactures iontophoresis devices designed to treat localized hyperhidrosis, including excessive sweating of the hands, feet, and underarms. The portfolio includes models such as the I2M.A and the IDROSTAR series, which deliver controlled electrical currents to reduce sweat production in targeted areas.

These devices fall under EU Class IIa classification and are registered in the EUDAMED database. The company is based in France and adheres to regulatory requirements for medical devices within the European Union.

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

Frequently asked questions

What medical devices does Laboratoires I2M manufacture?

Laboratoires I2M manufactures iontophoresis devices designed to treat localized hyperhidrosis, including excessive sweating of the hands, feet, and underarms. Their product portfolio includes models such as the I2M.A and the IDROSTAR series, which deliver controlled electrical currents to reduce sweat production in targeted areas.

Where is Laboratoires I2M based?

Laboratoires I2M is based in France, as indicated by the country code 'FR' in their device registration information. The company operates within the European Union and adheres to regulatory requirements for medical devices in that region.

Which regulatory registries list Laboratoires I2M's devices?

Laboratoires I2M's devices are listed in the EUDAMED database, which is the European Union's medical device database. This registry provides information about medical devices authorized for use in the EU market, including their classification and manufacturer details.

How are Laboratoires I2M's devices classified?

Laboratoires I2M's devices are classified as Class IIa under the EU medical device classification system. This classification indicates that these devices pose a moderate risk and require stricter controls than Class I devices, but less stringent requirements than Class IIb or Class III devices.

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

Information

Country
France
Address
16 bis, Fossés saint julien, CAEN, France
Phone
+33231502930
PRRC contact
Philippe DESNOS
EUDAMED SRN
FR-MF-000000296