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EUDAMED last updated this device on May 20, 2026
599302640CMYPY05993023041042 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Medicontur Medical Engineering Ltd.. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05993023041042599302640CMYPY05993023041042(01)05993023041042
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.
P030102100202IOLs, APHAKIC, MULTIFOCAL, ASPHERIC, 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 France; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Still on market | |
| Poland | 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.2023-MDR/QS-048/A2023-MDR/TD-048/A