- Role
- Country
- Date of registration
- Address
PL-MF-000028388No 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.Probówki typu Eppendorf o poj. 2 ml, z zamknięciem SAFE LOCK, z dnem soczewkowym, z podziałką i polem do opisu, o podwyższonej przezroczystości, bezbarwne, z PP is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Apr 16, 2026
5905072235041YXPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05905699564121
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.
05905699564121Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
5905072235041YX25-2000-1LUDI 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.
W05020199SAMPLES TRANSPORT, CONTAINERS - OTHER5905072235041YXOn the marketProbówki typu Eppendorf o poj. 2 ml, z dnem soczewkowym, z podziałką i polem do opisu, o podwyższonej przezroczystości, bezbarwne, z PP5905072235041YXOn the marketProbówki typu Eppendorf o poj. 2 ml, z dnem soczewkowym, z podziałką i polem do opisu, o podwyższonej przezroczystości, bezbarwne, z PP5905072235041YXOn the marketProbówki typu FALCONE o poj. 50ml, z czerwoną zakrętką, samostojące, sterylne, pakowane indywidualnieB-05905699560987On the marketProbówki typu FALCONE o poj. 50ml, z czerwoną zakrętką, sterylne, pakowane indywidualnieB-05905699560970On the marketProbówki typu FALCONE o poj. 50ml, z niebieską zakrętką5905072235039ZCOn the market