BEUDAMED
    13 results · 20ms · Sources: EU EUDAMED, US FDA

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    VYGON PREMI-CATH - LONG TERM CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    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

    DUPONT DIMENSION(R) ETHYL ALCOHOL(ALC) METHOD

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    GEN-X 800/650

    FDA 510(k)
    FDA Class 1 ·Radiology

    LIFEVEST WCD 4000

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·January 9, 2013

    OT VERIO IQ METER

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

    ASR ACETABULAR CUPS 58

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

    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