- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Sep 26, 2025
805228320R9002WVIT-MF-000032617No 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 Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
(01)18052283205411
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.
R9002LARYNGOSCOPE BLADES, SINGLE-USE