- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jan 5, 2023
73501429921010MZ21012 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Adaptis Spektra AB. Placed on the EU market in Sweden. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0735014299065773501429921010MZ21012(01)07350142990657
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.
V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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-000025764No 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.