- Role
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- Date of registration
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EUDAMED last updated this device on May 26, 2026
6944262907A0400VJTA6-200 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Wenzhou K.L.F. Medical Plastics Co., Ltd. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
069442629226846944262907A0400VJTA6-200(01)06944262922684
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.
A060102SURGICAL DRAINAGE CONNECTION MEDICAL TUBES7 warnings recorded — scroll inside the panel to see all entries.
CW275CW010CW009CW001CW007CW032CW136No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary 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.