- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Mar 30, 2026
5907568760710890UKSzkiełka mikroskopowe podstawowe ze szkła białego is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Lab Path Experts Paweł Piotrowski. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
59075687600160710890(01)59075687600160
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0503900201MICROSCOPE SLIDESPL-MF-000044413The 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.
Placed on the market in Poland; per-country availability dates not published.
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 →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 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.5905265530PHC95COn the marketParaffin for histology 56-58 deg C, without DMSO5905265530PHC95COn the marketParaffin for histology without DMSO, 54-56 deg C5905265530PHC95COn the marketTissue embedding mold 15 x 15 x 7 mm59052655307020SCOn the marketTissue embedding mold 24 x 24 x 7 mm59052655307020SCOn the marketTissue embedding mold 24 x 30 x 7 mm59052655307020SCOn the marketNo certificate specifically references this device's Basic UDI-DI.