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IGEA S.p.A.

Italy·IT-MF-000011242

Last updated September 17, 2026

What IGEA S.p.A. makes

IGEA S.p.A. manufactures the EPSA Series of medical devices, which appear to include a range of electrostimulation systems for therapeutic applications, as well as the JoCare device, likely a portable electrotherapy unit for muscle stimulation or pain management. These products are designed for clinical and home-use settings to support physical rehabilitation and recovery.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class IIa devices, indicating moderate risk and requiring compliance with specific safety and performance standards. These devices are registered in the EU’s eudamed database, ensuring traceability and transparency in the regulatory framework. The manufacturer is based in Italy.

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 IGEA S.p.A. manufacture?

IGEA S.p.A. specializes in electrostimulation systems, including the EPSA Series, which appears to cover a range of therapeutic electrostimulation devices. They also produce the JoCare device, likely a portable electrotherapy unit for muscle stimulation or pain relief. These products are designed for both clinical and home-use settings to aid in physical rehabilitation and recovery.

Where is IGEA S.p.A. based?

IGEA S.p.A. is based in Italy, as indicated by its country of origin. The company’s headquarters and manufacturing operations are located within the country.

Which regulatory registries list IGEA S.p.A.’s medical devices?

IGEA S.p.A.’s devices are registered in the eudamed database, which is the official EU registry for medical devices under the EU Medical Device Regulation (MDR). This ensures compliance and traceability for its products within the European market.

How are IGEA S.p.A.’s devices classified under EU regulations?

IGEA S.p.A.’s devices are classified as Class IIa under the EU Medical Device Regulation (MDR). This classification indicates a moderate risk level, requiring compliance with stricter safety and performance standards compared to lower-risk devices, such as Class I.

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

Information

Country
Italy
Address
10A, Via Parmenide, Carpi, Italy
LinkedIn
—
Facebook
—
Phone
+39059699600
PRRC Contact
Matteo Cadossi
EUDAMED SRN
IT-MF-000011242
FDA FEI Number
—
DUNS Number
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Catalogue (7)

DeviceModel / ReferenceRegistriesClassStatus
EPSA Series IGE060
EUDAMED
Class IIaActive
JoCare IG4800V
EUDAMED
Class IIaActive
EPSA Series IG0E080
EUDAMED
Class IIaActive
EPSA Series IG0E050
EUDAMED
Class IIaActive
EPSA Series IG0E090
EUDAMED
Class IIaActive
EPSA Series IG0E070
EUDAMED
Class IIaActive
EPSA Series IG0E040
EUDAMED
Class IIaActive

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