- Role
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- Date of registration
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EUDAMED last updated this device on May 28, 2026
5905072235067ZHMikrokońcówki o poj. 0.1-10µl, typu Gilson Pipetman, ze znacznikami 2 i 10µl, bezbarwne, 96 szt. w pudełku 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.
PL-MF-000028388Primary 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.
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.(01)05905699563841
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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.
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.
Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
05905699563841Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
5905072235067ZH80-0011-8EUDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0503020202PIPETTES, TIPS WITHOUT FILTER5905072235067ZHOn the marketMikrokońcówki o poj. 0.1-10µl, typu Eppendrof Crystal, bezbarwne, 96 szt. w pudełku5905072235067ZHOn the marketMikrokońcówki o poj. 0.1-10µl, typu Gilson Pipetman, ze znacznikami 2 i 10µl, bezbarwne5905072235067ZHOn the marketMikrokońcówki o poj. 0.1-10µl, typu Gilson Pipetman, ze znacznikami 2 i 10µl, bezbarwne, 96 szt. w pudełku5905072235067ZHOn the marketNaczynka do analizatorów HITACHI, z PS, o poj. 3ml5905072235042YZOn the marketPipetki Pasteura o poj. 1ml, dł. 15cm, z podziałką 1/0,25ml; z PE5905072235047ZBOn the market