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EUDAMED last updated this device on Apr 22, 2026
8591285UPLM3B38591285962579 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by MAXIS a.s.. Placed on the EU market in Czechia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
085912859625798591285UPLM3B38591285962579(01)08591285962579
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.
M030405COMPRESSION STOCKINGSNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Czechia; available across 6 countries total.
| Country | On market since | Until |
|---|---|---|
| CzechiaPrimary placement | Still on market | |
| Germany | Still on market | |
| France | Still on market | |
| Hungary | Still on market | |
| Poland | Still on market | |
| Slovakia | Still on market |
CZ-MF-000000989No 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.