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EUDAMED last updated this device on May 25, 2026
6944262906B0901WB50200 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Wenzhou K.L.F. Medical Plastics Co., Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069442629124876944262906B0901WB50200(01)06944262912487
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.
A03020102HIGH PRESSURE EXTENSION LINES7 warnings recorded — scroll inside the panel to see all entries.
CW275CW010CW009CW001CW007CW032CW136No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Dec 8, 2022 | Dec 31, 2036 |
CN-MF-000011214No 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.