BEUDAMED
    5,653 results · 30ms · Sources: EU EUDAMED, US FDA

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    Resection Guide KHO KLA

    FDA UDI
    ENZTEC LIMITED·09421028115995·A reusable manual surgical instrument intended ...

    CORAIL AMT NECK SEG 135D KHO

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LXH·May 14, 2025

    CORAIL2 NON COL HO SIZE 13

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS - 3003895575·Product code KWA·October 16, 2019

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 16, 2019

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORPORATION·Product code FPA·June 18, 2012

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code KXA·December 11, 2019

    CORAIL AMT COLLAR SIZE 9

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS REG. # 3003895575·Product code KWY·December 6, 2013

    ACESSA PROVU HANDPIECE

    FDA Adverse Event
    Injury ·ACESSA HEALTH INC.·Product code HFG·November 8, 2021

    CORAIL AMT NECK SEG 135D KHO

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LXH·March 10, 2025

    CORAIL AMT NECK SEG 135D KHO

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS - 3003895575·Product code LXH·January 5, 2021

    CORAIL2 NON COL HO SIZE 12

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS INC US·Product code LZO·October 28, 2025

    CORAIL2 NON COL HO SIZE 14

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS - 3003895575·Product code KWL·September 25, 2019

    CORAIL AMT SZ10 135 HIGH COL

    FDA Adverse Event
    Malfunction ·DEPUY FRANCE SAS - 3003895575·Product code JDI·November 13, 2019

    UNKNOWN CORAIL KHO STEM

    FDA Adverse Event
    Injury ·3003895575 DEPUY FRANCE S.A.S.-SAINT PRIEST·Product code KWL·April 12, 2017

    PERFECTA(R) FEMORAL STEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDI·December 14, 2012

    LINEAGE® TRANSCEND® CERAMIC FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·December 14, 2012

    LINEAGE® TRANSCEND® CERAMIC ACETABULAR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·December 14, 2012

    LINEAGE® SHELL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·December 14, 2012

    LINEAGE® SHELL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDI·December 14, 2012

    LINEAGE® TRANSCEND® CERAMIC ACETABULAR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·December 14, 2012