- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 21, 2026
8588010113RECTOVENALNFSK-MF-000001981No 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.
CW011Primary placement in Slovakia; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| SlovakiaPrimary placement | May 22, 2015 | Still on market |
(01)08588006802283
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.
M9002PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)