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EUDAMED last updated this device on Apr 25, 2026
4031881G10-01IIaKB911792S is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by KD Medical GmbH Hospital Products. Placed on the EU market in Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
140318819117994031881G10-01IIaKB911792S(01)14031881911799
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
A0101010101HYPODERMIC SYRINGE NEEDLES, WITH SAFETY SYSTEMS5 warnings recorded — scroll inside the panel to see all entries.
CW011CW009CW001CW007CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 13 countries total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Jan 18, 2024 | Still on market |
| Bulgaria | Jan 18, 2024 | Still on market |
| Czechia | Jan 18, 2024 | Still on market |
| Germany | Jan 18, 2024 | Still on market |
| Denmark | Jan 18, 2024 | Still on market |
| Finland | Jan 18, 2024 | Still on market |
| France | Jan 18, 2024 | Still on market |
| Croatia | Jan 18, 2024 | Still on market |
| Netherlands | Jan 18, 2024 | Still on market |
| Norway | Jan 18, 2024 | Still on market |
| Portugal | Jan 18, 2024 | Still on market |
| Sweden | Jan 18, 2024 | Still on market |
| Slovakia | Jan 18, 2024 | Still on market |
DE-MF-000006773No 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.