BEUDAMED
    23 results · 25ms · Sources: EU EUDAMED, US FDA

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    NOVEL III SPINAL FIXATION AND ADJUSTABLE BRIDGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517563941·CoRoent Ant TLIF PEEK, 11x10x28mm 4°

    LIQUIBAND ULTIMA, LUT 003

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

    LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)

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

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    CAIMAN DISP. INSTR. NON ARTICUL.D:5 / 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 18, 2016

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/ 360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·July 22, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·February 27, 2015

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·May 13, 2013

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·June 1, 2011

    HITACHI 917 DISK

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 14, 2008

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·April 20, 2016

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·March 4, 2015

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·February 17, 2016

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 22, 2020

    Video Duodenoscope

    FDA Enforcement
    Class II ·Terminated·Pentax Medical Company·June 8, 2016