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ACTION SPÓŁKA AKCYJNA

PL-MF-000046182 · Poland · ZAMIENIE

ACTION SPÓŁKA AKCYJNA is registered in the European database on medical devices as a manufacturer, with 72 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa72

Most frequent device types declared: PRIMO.

Among these devices, 7 are declared active.

Devices declared under this manufacturer

Showing 12 of 72 declared devices.

Catalogue references include B300AM, KP600AM, LR300AM, LW200AM, M100AM, NT10AM.

European nomenclature codes declared: Y093303, Y120606, Y091209, V080399, Y120399, V08060101.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED72
Country of registrationPoland

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

Device-level evidence

Devices with a numeric GTIN72
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. ACTION SPÓŁKA AKCYJNA was not found in either the U.S. or the Canadian register.

Other manufacturers in Poland

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