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- Date of registration
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EUDAMED last updated this device on Feb 2, 2026
803413929UNICO1aRFIT-MF-000019320803413929UNICO1aRFOn the marketUNICO - PERCUTANEOUS KIT CH 15 WITH EXTENSION LINE803413929UNICO1aRFOn the marketUNICO MULTI-J - PERCUTANEOUS KIT SELDINGER CH 9803413929UNICO1aRFOn the marketUNICO XL - PERCUTANEOUS KIT CH12803413929UNICO1aRFOn the marketUNICO "FORTY" - PERCUTANEOUS KIT CH 9 WITH EXTENSION LINE803413929UNICO1aRFOn the marketNo 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.6 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW001CW020CW032CW007Primary placement in Italy; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 3, 2011 | Still on market |
| Germany | Jan 3, 2011 | Still on market |
| Spain | Jan 3, 2011 | Still on market |
| France | Jan 3, 2011 | Still on market |
| Poland | Jan 3, 2011 | Still on market |
(01)08034139296944
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.
A060204THORACENTESIS AND PARACENTESIS DRAINAGES AND KITS