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

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    WART FREEZE

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

    GMK HINGE FEMUR SIZE 2 RIGHT

    FDA Adverse Event
    Injury ·Product code KRO·September 12, 2014

    CAS FIXATION PIN 3.2 DIA X 180 MM STR, CAS FIXATON PIN 3.2 DIA X 80 MM STR, CAS FIXATON PIN 3.2 DIA X 150 MM

    FDA 510(k)
    FDA Class 2 ·Neurology

    UNIVERSAL DIGITAL INTERFACE (UDI) 1717

    FDA 510(k)
    FDA Class 2 ·Radiology

    GMK HINGE FEMUR SIZE 5 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

    GMK HINGE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·September 4, 2025

    GMK HINGE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·May 13, 2026

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 12, 2015

    GMK HINGE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·December 30, 2025

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    GMK-HINGE FIXED TIBIAL TRAY SIZE 4 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·October 29, 2020

    GMK-HINGE 02.09.0523H FIXED TIBIAL INSERT SIZE 5/23MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·October 6, 2023

    CAIMAN DISP. INSTR. ARTICULAR D-12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·May 6, 2014

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

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL S.A.·Product code GEI·March 21, 2014

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014

    GMK-HINGE FEMORAL COMPONENT SIZE 2 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·June 28, 2019

    GMK-HINGE FIXED TIBIAL INSERT SIZE 1/26MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·July 12, 2019

    GMK-HINGE FEMORAL COMPONENT SIZE3 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·December 20, 2021

    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