- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Nov 15, 2025
5600760338STPRESEFPT-MF-000040052No 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.3 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW030Primary placement in Portugal; available across 1 country total.
Placed on the market in Portugal; per-country availability dates not published.
(01)05600760338471
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.
V0804PATIENT IMMOBILISERS (in diagnostic or therapeutic procedures)