BEUDAMED
    8 results · 34ms · Sources: EU EUDAMED, US FDA

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    SEER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LOQTEQ VA Calcaneus Plate 3.5

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SUBCUTANEOUS NEEDLE INFUSION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 9, 2023

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·April 10, 2014

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIVISION·Product code INK·October 21, 2010

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 20, 2012

    PICCO MONITORING KIT

    FDA Adverse Event
    Malfunction ·PULSION MEDICAL SYSTEMS SE·Product code KRB·September 23, 2022