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313 Spółka z ograniczoną odpowiedzialnością

PL-MF-000043637 · Poland · Białystok

313 Spółka z ograniczoną odpowiedzialnością is registered in the European database on medical devices as a manufacturer, with 55 devices declared. It was not found in the U.S. FDA device establishment register.

What this manufacturer declares

Class IIa55

Most frequent device types declared: CLASSIC, COHESIVE, DOUBLE, PREMIUM, REA POWER BAND.

Devices declared under this manufacturer

Showing 12 of 55 declared devices.

Catalogue references include 41, 70, 71, RE/CO/BK/545, RE/CO/OR/545/OU, RE/CO/YL/545/PTH.

European nomenclature codes declared: M0303010203, V0899, Z12069099, Y093303, Q010599, M9099.

United States market access

FDA establishment registerNot found in the FDA register
Devices in EUDAMED55
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 GTIN55
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. 313 Spółka z ograniczoną odpowiedzialnością was not found in either the U.S. or the Canadian register.

Other manufacturers in Poland

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