BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Bakri Essential Postpartum Balloon

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ACCUFUSER, ACCUFUSER PLUS, STANDARD PROCEDURE KIT, ACCUFUSER INFUSION KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    XGEO GC80

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD BBL¿ SABOURAUD AGAR W CHLORAMPHENICOL, PLATE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON GMBH·Product code JSJ·November 9, 2021

    CONICAL EXTRACTION SCREW FOR 2.7MM & 3.5MM CORTEX SCREWS

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWB·September 16, 2020

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·August 10, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·November 4, 2014

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 12, 2013

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018