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Lab Path Experts Paweł Piotrowski

PL-MF-000044413 · Poland · Koziegłowy

Lab Path Experts Paweł Piotrowski is registered in the European database on medical devices as a manufacturer, with 17 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa2

Most frequent device types declared: Microscope slides.

Among these devices, 2 are declared active.

Devices declared under this manufacturer

Showing 12 of 17 declared devices.

Catalogue references include 702035, 702036, 702037, 710190, 710290, 710890.

European nomenclature codes declared: W0202059099, W01030704, W0503900201, W0202059012, W02079001.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED17
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 GTIN17
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. Lab Path Experts Paweł Piotrowski was not found in either the U.S. or the Canadian register.

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