- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jun 28, 2024
594067440RECOLT.VIDATEBARO-MF-000037201594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amikacin, AK, 10mcg594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amikacin, AK, 30mcg594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amoxycillin, AMX, 10mcg594067440SUSCEPT.DISCSZKOn the marketDiscs for antimicrobial susceptibility testing Amoxycillin, AMX, 25mcg594067440SUSCEPT.DISCSZKOn the marketNo 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.1 warning recorded — scroll inside the panel to see all entries.
CW010Primary placement in Netherlands; available across 1 country total.
Placed on the market in Netherlands; per-country availability dates not published.
(01)05940674402050
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.
W050101010201BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR