BEUDAMED
    25 results · 24ms · Sources: EU EUDAMED, US FDA

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    RESPIRONICS SILHOUETTE NASAL MASK, MODELS 1003224 AND 1003223

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Leksell Stereotactic System

    FDA UDI
    Elekta Instrument AB·07340048305181·ARC SUPPORT LEFT

    ODYSSEY®

    FDA UDI
    Microport Orthopedics Inc.·M684K00007051·

    TEWA

    FDA UDI
    asia-med GmbH·04251282512828·TeWa PB-Type 3030: coated acupuncture needles ...

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282505837·TeWa PB-Type 3030: coated acupuncture needles ...

    BMA Kit

    FDA UDI
    Biomet Biologics, LLC·00880304451759·

    Single Use Biliary Stent V

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170185397·

    FlowLogic Assert

    FDA UDI
    SONENDO, INC.·00810209420543·FlowLogic Assert Shaping File 15/.06, 21mm

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 30, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 30, 2026

    MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),

    FDA 510(k)
    FDA Class 2 ·Neurology

    IMMULITE VALPROIC ACID, IMMULITE 2000 VALPROIC ACID, CATALOG # LKVA1, LKVA5 & L2KVA2, L2KVA6

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 30, 2026

    INSET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 30, 2026

    AISYS

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 15, 2016

    DOUBLE FENESTRATED GRASPER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·March 12, 2013

    VASOVIEW HEMOPRO 2 EVH SYSTEM

    FDA Adverse Event
    Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·February 8, 2011

    LIFEPAK 12 DIFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·February 19, 2008

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 12, 2018

    PROMUS ELEMENT EVEROLIMUS-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 12, 2018