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KEROX Ipari és Kereskedelmi Korlátolt Felelősségű Társaság

HU-MF-000031741 · Hungary · Sóskút

KEROX Ipari és Kereskedelmi Korlátolt Felelősségű Társaság is registered in the European database on medical devices as a manufacturer, with 3 207 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa3 207

Among these devices, 40 are declared reusable, 2 137 active.

Devices declared under this manufacturer

Showing 12 of 3 207 declared devices.

Catalogue references include CA1W0014DM, CA2U7122AG, CA4Z0010DM, CB2C9512ZZ, CC3C7125AG, CH4E7110AG.

European nomenclature codes declared: Q010699.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED3 207
Country of registrationHungary

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

Device-level evidence

Devices with a numeric GTIN3 207
Found in the U.S. device database0
Share0.0 %

Canadian market access

Health Canada licence listingNot found in the Canadian register

⚠️ Canada lists no Class I devices at all — what that excludes.

North American profile: Neither register. KEROX Ipari és Kereskedelmi Korlátolt Felelősségű Társaság was not found in either the U.S. or the Canadian register.

Other manufacturers in Hungary

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