BEUDAMED
    13 results · 38ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    GAMP & ASSOC. DISPOSABLE ENDOOCULAR LASER PROBE

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    DUPONT SALICYLATE CALIBRATOR

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    KONTRON DEFIBRILLATOR 7501

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·May 22, 2015

    PREMICATH

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH

    FDA Adverse Event
    VYGON GMBH·Product code LJS·April 20, 2015

    PREMICATH PICC

    FDA Adverse Event
    Malfunction ·VYGON GMBH·Product code LJS·June 3, 2015

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·January 9, 2013

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code KWA·January 5, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2014

    23GA ILLUMINATED DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·March 19, 2020

    25GA ILLUMINATED DIRECTIONAL LASER PROBE

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQB·March 19, 2020