BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    COAXIAL APPLICATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ormco

    FDA UDI
    ORMCO CORPORATION·00889989026856·ARCH P/F EDG.RECT.LO170 X220 PK10

    AGILENT COMPONENT MONITORING SYSTEM; AGILENT INVASIVE BLOOD PRESSURE MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATRICURE BIPOLAR COAGULATION SYSTEM

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

    NEB100

    FDA Adverse Event
    Malfunction ·SUNSET HEALTHCARE SOLUTIONS·Product code CAF·January 29, 2019

    OXF UNI TIB TRAY SZ B RM PMA

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·May 3, 2013

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 20, 2014

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 17, 2011