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

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    MARCO STANDARD KERATOMETERS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    PRE-POWDERED LATEX ORTHOPEDIC SURGEON'S GLOVES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    H-30 HOLMIUM LASER SYSTEM

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

    IBOND TOTAL ETCH

    FDA Adverse Event
    Injury ·HERAEUS KULZER GMBH·Product code KLE·January 9, 2013

    EQUASHIELD

    FDA Adverse Event
    EQUASHIELD MEDICAL LTD.·Product code LHI·October 26, 2010

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 11, 2014

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·October 30, 2017

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·February 9, 2018

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·February 28, 2018

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GEX·February 8, 2018

    H30 HOLMIUM LASER 30 WATT HOLMIUM LASER

    FDA Adverse Event
    Injury ·COOK INC·Product code GEX·April 25, 2018