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EUDAMED last updated this device on May 12, 2026
69422750MCK1RFLENSE AMNA is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Gansu Constar Technology Group Co., Ltd.. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0694267150079069422750MCK1RFMCK1(01)06942671500790
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.
Q0210040102CONTACT LENSES - HYDROGEL, REUSABLE1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 12 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | May 12, 2026 | May 11, 2027 |
| Austria | May 12, 2026 | May 11, 2027 |
| Belgium | May 12, 2026 | May 11, 2027 |
| Denmark | May 12, 2026 | May 11, 2027 |
| Spain | May 12, 2026 | May 11, 2027 |
| Finland | May 12, 2026 | May 11, 2027 |
| France | May 12, 2026 | May 11, 2027 |
| Italy | May 12, 2026 | May 11, 2027 |
| Netherlands | May 12, 2026 | May 11, 2027 |
| Poland | May 12, 2026 | May 11, 2027 |
| Romania | May 12, 2026 | May 11, 2027 |
| Sweden | May 12, 2026 | May 11, 2027 |
CN-MF-000041579No 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.