EU → North America Device Access

Cedic srl

IT-MF-000019323 · Italy · Peschiera Borromeo

Cedic srl is registered in the European database on medical devices as a manufacturer, with 63 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa63

Among these devices, 38 are declared sterile.

Devices declared under this manufacturer

Showing 12 of 63 declared devices.

Catalogue references include 12267446, 12309180, 12440917, 12459535, 589734, 777555.

European nomenclature codes declared: A030403, A070199, A080101, A030499, G02020102, A0680.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED63
Country of registrationItaly

⚠️ Not found is not the same as not sold — how this comparison can be wrong.

Device-level evidence

Devices with a numeric GTIN62
Found in the U.S. device database6
Share9.7 %
⚠ The two levels disagree here. This company’s name was not found in the FDA establishment register, yet some of its devices are in the U.S. device database. The likeliest reading is that the name match failed.

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entryCEDIC SRL

What it holds in Canada

Licences on record1
Currently active0
Class 2 devices1
First licensed2015-09-15

Licence types: Device Family (1).

Licensed under: ENFIT TRANSITION CONNECTORS FOR ENTERAL APPLIC.

North American profile: Canada only. Cedic srl holds a Canadian licence but was not found in the U.S. register.

Other manufacturers in Italy

All Italy manufacturers →