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- Date of registration
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EUDAMED last updated this device on May 20, 2026
697156463XRTATLH6884X is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIb. Manufactured by Hangzhou Kailong Medical Instruments Co., Ltd.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06971564630948697156463XRTATLH6884-0.6/1.2-150-V1(01)06971564630948
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.
Z11039012X-RAY TUBE ASSEMBLYNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Jan 1, 2026 | Dec 31, 2099 |
CN-MF-000030241No 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.