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EUDAMED last updated this device on Jun 4, 2026
69383279204XF0693832790199869383279204XFDRT-SK501FC(01)06938327901998
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.
A02010401SYRINGES FOR CONTRAST MEDIA INJECTOR, SINGLE-USE1 warning recorded — scroll inside the panel to see all entries.
CW999No 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 | Mar 7, 2024 | Dec 31, 2099 |
CN-MF-000018400No 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.69383279217XQOn the marketMulti-Use Tubing System Kit69383279217XQOn the marketSingle-use Sterile High-pressure Angiographic Syringes and Accessories69383279203XDOn the marketSingle-use Sterile High-pressure Angiographic Syringes and Accessories69383279203XDOn the marketSingle-use Sterile High-pressure Angiographic Syringes and Accessories69383279206XKOn the market