BEUDAMED
    7 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    MODEL 1350 URODYNAMIC WAVEFORM PROCESSOR

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    EMMA ANALYZER (KPA) AND (MMHG); EMMA MONITOR (KPA) AND (MMHG)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CKS Plus Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ISA CO2

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 30, 2022

    SECURA DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·June 10, 2014

    CONSULTA

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NIK·October 9, 2010

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 10, 2012