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- Date of registration
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EUDAMED last updated this device on Apr 23, 2023
73500849764984LGB-2023-01/DE-2023-01 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Nordic activity AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0735008497649873500849764984LGB-2023-01/DE-2023-01(01)07350084976498
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.
Y120699WALKING DEVICES, TWO-HANDED OPERATION - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Sweden; available across 1 country total.
Placed on the market in Sweden; per-country availability dates not published.
SE-MF-000002371No 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.