- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Feb 26, 2026
8719324589RDCJUNL-MF-000026292No 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.Primary placement in Netherlands; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Feb 24, 2023 | Feb 1, 2028 |
| Austria | Feb 24, 2023 | Feb 1, 2028 |
| Belgium | Feb 24, 2023 | Feb 1, 2028 |
| Bulgaria | Feb 24, 2023 | Feb 1, 2028 |
| Cyprus | Feb 24, 2023 | Feb 1, 2028 |
| Czechia | Feb 24, 2023 | Feb 1, 2028 |
| Germany | Feb 24, 2023 | Feb 1, 2028 |
| Denmark | Feb 24, 2023 | Feb 1, 2028 |
| Estonia | Feb 24, 2023 | Feb 1, 2028 |
| EL | Feb 24, 2023 | Feb 1, 2028 |
| Spain | Feb 24, 2023 | Feb 1, 2028 |
| Finland | Feb 24, 2023 | Feb 1, 2028 |
| France | Feb 24, 2023 | Feb 1, 2028 |
| Croatia | Feb 24, 2023 | Feb 1, 2028 |
| Hungary | Feb 24, 2023 | Feb 1, 2028 |
| Ireland | Feb 24, 2023 | Feb 1, 2028 |
| Iceland | Feb 24, 2023 | Feb 1, 2028 |
| Italy | Feb 24, 2023 | Feb 1, 2028 |
| Liechtenstein | Feb 24, 2023 | Feb 1, 2028 |
| Lithuania | Feb 24, 2023 | Feb 1, 2028 |
| Luxembourg | Feb 24, 2023 | Feb 1, 2028 |
| Latvia | Feb 24, 2023 | Feb 1, 2028 |
| Malta | Feb 24, 2023 | Feb 1, 2028 |
| Norway | Feb 24, 2023 | Feb 1, 2028 |
| Poland | Feb 24, 2023 | Feb 1, 2028 |
| Portugal | Feb 24, 2023 | Feb 1, 2028 |
| Romania | Feb 24, 2023 | Feb 1, 2028 |
| Sweden | Feb 24, 2023 | Feb 1, 2028 |
| Slovenia | Feb 24, 2023 | Feb 1, 2028 |
| Slovakia | Feb 24, 2023 | Feb 1, 2028 |
| Türkiye | Feb 24, 2023 | Feb 1, 2028 |
| XI | Feb 24, 2023 | Feb 1, 2028 |
(01)08719324589017
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.
Z11029005AUTOMATIC DOSE CALIBRATORS