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EUDAMED last updated this device on May 28, 2026
5905072235068ZKGranulat do separacji surowicy - 300g is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by MEDLAB-PRODUCTS Sp. z o.o.. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0590569956057432-9300-0(01)05905699560574
European Medical Device Nomenclature — the EU product classification assigned to this device.
W050301029001BLOOD COMPONENTS SEPARATORS, PLASTICPL-MF-000028388No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificate specifically references this device's Basic UDI-DI.
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | — | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
View in glossary →B-05905699561960On the marketEzy z oczkiem o poj. 1µl, z PS, żółte, pakowane po 20szt w pudełko z dozownikiem - sterylneB-05905699561977On the marketGranulat do separacji surowicy - 1000g5905072235068ZKOn the marketGranulat do separacji surowicy - 600g5905072235068ZKOn the marketKońcówki o poj. do 1000µl, typu Eppendorf, klasa Economy, bezbarwne5905072235067ZHOn the marketKońcówki o poj. do 1000µl, typu Eppendorf, klasa Economy, niebieskie5905072235067ZHOn the market