- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 21, 2026
599302677CMTYP305993023045750599302677CMTYP305993023045750(01)05993023045750
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.
P030102100302IOLs, APHAKIC, MULTIFOCAL, TORIC, HYDROPHILIC ACRYLIC5 warnings recorded — scroll inside the panel to see all entries.
CW001CW007CW009CW010CW011No certificate specifically references this device's Basic UDI-DI.
Primary placement in Czechia; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| CzechiaPrimary placement | Still on market | |
| Belgium | Still on market | |
| Germany | Still on market | |
| Spain | Still on market | |
| France | Still on market | |
| Italy | Still on market | |
| Latvia | Still on market | |
| Netherlands | Still on market | |
| Poland | Still on market | |
| Romania | Still on market |
HU-MF-000024195No 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.