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EUDAMED last updated this device on Jun 3, 2026
8018294P0513EM_F100022P0513EM F1000 REF 1 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by FLAEM NUOVA SpA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080182940161358018294P0513EM_F100022P0513EM F1000 REF 1(01)08018294016135
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.
Z12159002AEROSOL EQUIPMENT1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market |
IT-MF-000007769No 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.