EU → North America Device Access

CuraMedical B.V.

NL-MF-000000052 · Netherlands · Assendelft

CuraMedical B.V. is registered in the European database on medical devices as a manufacturer, with 39 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class I38
Class IIb1

Most frequent device types declared: CC-501, CC-503, CC-503-C, CC-510-C, CC-537.

Among these devices, 39 are declared sterile, 39 implantable.

Catalogue references include CC-501, CC-503, CC-503-C, CC-510-C, CC-537, CH-603.

European nomenclature codes declared: M040501, M040506.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED39
Country of registrationNetherlands

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

Device-level evidence

Devices with a numeric GTIN39
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. CuraMedical B.V. was not found in either the U.S. or the Canadian register.

Other manufacturers in Netherlands

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