EU → North America Device Access

INTERMED SRL

IT-MF-000013039 · Italy · MILANO

INTERMED SRL is registered in the European database on medical devices as a manufacturer, with 97 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa97

Most frequent device types declared: AUSILI BAGNO, AUSILI DEAMBULAZIONE, AUSILI ORTOPEDICI, CARROZZINE, CARROZZINE ELETTRICHE.

Devices declared under this manufacturer

Showing 12 of 97 declared devices.

Catalogue references include AD-91-R, CL-42-GREEN, E-LIGHT+40T, E-LIGHT+42T, PW-M10B-51, PW-M10G-44.

European nomenclature codes declared: Y122103, Y122127, Y122106, Y122406, Y12030602, Y093303.

United States market access

FDA establishment registerRegistered with FDA
Matched entryINTER-MED, INC. (US) · FDA 2133714
Devices in EUDAMED97
Country of registrationItaly

Device-level evidence

Devices with a numeric GTIN97
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryINTER-MED, INC.

What it holds in Canada

Licences on record39
Currently active0
Class 2 devices28
Class 3 devices11
First licensed2005-08-26

Licence types: Device Family (17), Device Group Family (10), System (5), Device Group (4).

Licensed under: SIMPLICITY, INTERFACE (CERAMIC/ENAMEL/DENTIN PRIMER), ASPIRATORS, ASPIRATING SYRINGE, SUCTION VALVES, AIR WATER SYRINGE.

North American profile: Both markets. INTERMED SRL is registered in both the United States and Canada.

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