- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 24, 2026
4031881G10-01IIaKB240318819006394031881G10-01IIaKB900635(01)24031881900639
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.
A0101010102HYPODERMIC SYRINGE NEEDLES, W/O SAFETY SYSTEMS4 warnings recorded — scroll inside the panel to see all entries.
CW011CW009CW001CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 14 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 |
| Romania | 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.