BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    PHOENIX ANESTHESIA MACHINE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209116126·

    Achieve ST Mapping Catheter, Catheter Connecting Cable

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FOTONA QX ND:YAG/KTP LASER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PALL TRANSFER/FREEZING BAG SET FOR PROCESSING AND FREEZING CORD BLOOD

    FDA Adverse Event
    Malfunction ·ENSATEC, S.A. DE C.V.·Product code KSR·December 23, 2009

    UNKNOWN DEPUY TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 6, 2014

    XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·November 30, 2012

    ALARIS® PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FPA·June 18, 2015

    Acumatch L-Series BIPOLAR LINER, 22mm (BIPOLAR ENDOPROSTHESIS-Hip), Item Numbers: a) 100-22-19, SZ. L; b) 100-22-20, SZ. M; c) 100-22-21, SZ. N; d) 100-22-22, SZ. P; e) 100-22-23, SZ. R; f) 100-22-24, SZ. S; g) 100-22-25, SZ. T

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·July 10, 2024