BEUDAMED
    43 results · 30ms · Sources: EU EUDAMED, US FDA

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    SOMNOLYZER 24X7

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LINVATEC 300W XENON LIGHT SOURCE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    APEX KNEE MODULAR TIBIA SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ZYDERM 1 COLLAGEN IMPLANT

    FDA Adverse Event
    Injury ·COLLAGEN CORP.·Product code LMH·December 14, 1998

    TSRH SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK MANUFACTURING·Product code KWQ·August 16, 2000

    SILTEX BECKER/EXPANDER MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·November 24, 1998

    UNKNOWN

    FDA Adverse Event
    Malfunction ·UNKNOWN·February 9, 1995

    UNKNOWN

    FDA Adverse Event
    Malfunction ·UNKNOWN·February 9, 1995

    GROSSE AND KEMPF NAIL

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HSB·August 22, 1997

    BARD

    FDA Adverse Event
    Injury ·BARD ACCESS SYSTEMS·Product code LJT·July 29, 1994

    INNER SHEATH, FOR 26 FR. OUTER SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·August 8, 2024

    GEL FILLED MAMMARY IMPLANT

    FDA Adverse Event
    Injury ·DOW CORNING CORP·Product code FTR·October 16, 1996

    DEVON

    FDA Adverse Event
    Malfunction ·DEVON INDUSTRIES·Product code GDJ·August 2, 1994

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·August 13, 2024

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011

    6F ANGIO-SEAL VIP VASCULAR CLOSURE DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL PUERTO RICO, B.V.·Product code MGB·August 21, 2008

    RESECTION SHEATH, 8 MM, FOR 8.5 MM/26 FR. OUTER SHEATH, ABS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·April 25, 2024

    BUTTRESS PLATE AND CHANNEL PLATE

    FDA Adverse Event
    Injury ·HOWMEDICA, INC.·Product code HRS·May 24, 1994

    INNER SHEATH, FOR 26 FR. OUTER SHEATH

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code HIH·August 6, 2024