BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    CLARUS ENDOSCOPIC BALL PROBE

    FDA 510(k)
    FDA Class 1 ·Neurology

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867138513·HOHMANN RETRTR,9.75" LGX 19MM WD BLADE

    DURACON ALL PLASTIC TIBIAL COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BP8800T/8000IR/8300G NON-INVASIVE BLOOD PRES. SYST

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOHMANN RETRTR,9.75" LGX 19MM WD BLADE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·June 5, 2024

    OXIMAX N-595 PULSE OXIMETER

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DQA·November 10, 2010

    LEAVE ACTIVE PFC STB 10MM SZ5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·January 23, 2013

    TENDRIL STS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014