BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    PORTABLE X-RAY SYSTEM, MODEL POWERMAX 1260

    FDA 510(k)
    FDA Class 2 ·Radiology

    PPCID- PNEUMATIC PERIPHERAL CIRCULATION IMPROVEMENT (FOOTREST) DEVICE

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    AT HOME DRUG TESTT, MODEL 9150 T

    FDA 510(k)
    FDA Unclassified ·Unknown

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DDD

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·December 29, 2015

    SELUTE PICOTIP

    FDA Adverse Event
    Death ·CPI - DEL CARIBE·Product code NVN·May 2, 2013

    LARGE MOD HEAD ADAPT 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·September 15, 2014

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 19, 2011

    Exactech Equinoxe GLENOID, POSTERIOR AUGMENT,PEGGED, CEMENTED, 8o, RIGHT, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-02-32, b) 41, 44, 47, 50 head, Medium, Item Number 314-02-33, c) 44, 47, 50, 53 head, Large, Item Number 314-02-34, d) 44, 47, 50, 53 head, Extra Large, Item Number 314-02-35; Shoulder Arthroplasty

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