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EUDAMED last updated this device on Mar 24, 2026
475102853REF532153K5REF532153 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Liepājas Speciālās ekonomiskās zonas SIA NordePlast. Placed on the EU market in Latvia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04751028532153475102853REF532153K5REF532153(01)04751028532153
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.
M0599MEDICAL PLASTERS - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Latvia; available across 1 country total.
Placed on the market in Latvia; per-country availability dates not published.
LV-MF-000026735No 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.