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EUDAMED last updated this device on Apr 30, 2025
872062130006AMNL-MF-000006042No 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.1 warning recorded — scroll inside the panel to see all entries.
CW007Primary placement in Netherlands; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Sep 18, 2024 | Aug 29, 2028 |
| Austria | Sep 18, 2024 | Aug 29, 2028 |
| Belgium | Sep 18, 2024 | Aug 29, 2028 |
| Bulgaria | Sep 18, 2024 | Aug 29, 2028 |
| Cyprus | Sep 18, 2024 | Aug 29, 2028 |
| Czechia | Sep 18, 2024 | Aug 29, 2028 |
| Germany | Sep 18, 2024 | Aug 29, 2028 |
| Denmark | Sep 18, 2024 | Aug 29, 2028 |
| Estonia | Sep 18, 2024 | Aug 29, 2028 |
| EL | Sep 18, 2024 | Aug 29, 2028 |
| Spain | Sep 18, 2024 | Aug 29, 2028 |
| Finland | Sep 18, 2024 | Aug 29, 2028 |
| France | Sep 18, 2024 | Aug 29, 2028 |
| Croatia | Sep 18, 2024 | Aug 29, 2028 |
| Hungary | Sep 18, 2024 | Aug 29, 2028 |
| Ireland | Sep 18, 2024 | Aug 29, 2028 |
| Iceland | Sep 18, 2024 | Aug 29, 2028 |
| Italy | Sep 18, 2024 | Aug 29, 2028 |
| Liechtenstein | Sep 18, 2024 | Aug 29, 2028 |
| Lithuania | Sep 18, 2024 | Aug 29, 2028 |
| Luxembourg | Sep 18, 2024 | Aug 29, 2028 |
| Latvia | Sep 18, 2024 | Aug 29, 2028 |
| Malta | Sep 18, 2024 | Aug 29, 2028 |
| Norway | Sep 18, 2024 | Aug 29, 2028 |
| Poland | Sep 18, 2024 | Aug 29, 2028 |
| Portugal | Sep 18, 2024 | Aug 29, 2028 |
| Romania | Sep 18, 2024 | Aug 29, 2028 |
| Sweden | Sep 18, 2024 | Aug 29, 2028 |
| Slovenia | Sep 18, 2024 | Aug 29, 2028 |
| Slovakia | Sep 18, 2024 | Aug 29, 2028 |
| Türkiye | Sep 18, 2024 | Aug 29, 2028 |
| XI | Sep 18, 2024 | Aug 29, 2028 |
(01)08720621323013
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.
C010402020101PTA BALLOON DILATATION CATHETERS