BEUDAMED
    9 results · 18ms · Sources: EU EUDAMED, US FDA

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    NIKOPAD ELECTROSURGICAL GROUNDING PAD (*OR SOLD UNDER COMMERCIAL NAMES), MODEL 4760 (TYPICALLY)

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

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993306·anteriors; shade C1; mould BOS

    PROView

    FDA 510(k)
    FDA Class 2 ·Radiology

    SINGLE-PATIENT USE DISPOSABLE SENSOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SYNERGY¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 4, 2015

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    JUMAO MEDICAL EQUIPMENT·Product code IOR·March 7, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 31, 2010

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    ENCOREANYWHERE

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·February 17, 2016