BEUDAMED
    340 results · 84ms · Sources: EU EUDAMED, US FDA

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    AS VEGA SYSTEM® PS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 13, 2026

    AS VEGA SYSTEM® PS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·March 12, 2026

    KNEE ENDOPROSTHETICS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code OOG·March 12, 2026

    Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint.

    FDA Enforcement
    Class II ·Terminated·Aesculap, Inc.·March 9, 2016

    KNEE ENDOPROSTHETICS

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·December 16, 2024

    PLASMACUP SC SIZE 52MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code LWJ·May 2, 2019

    PROGAV 2.0®

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO KG·Product code JXG·March 31, 2025

    Excia Cemented Hip Stems, Size 12mm, Part Number: NJ312K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 17mm, Part Number : NJ317K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 14mm, Part Number : NJ314K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems ,Size 18mm, Part Number NJ318K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 13mm, Part Number : NJ313K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 16mm, Part Number NJ316K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 9mm, Part Number: NJ309K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 11mm, Part Number : NJ311K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 10mm, Part Number: NJ310K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 15mm, Part Number: NJ315K Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    COLLECT.NO.QAS KNEE IMPL.MISC./UNKNOWN

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·February 19, 2021

    PROGAV 2.0 WITH PED.BURRHOLE RESERVOIR

    FDA Adverse Event
    Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·April 5, 2019

    COLLECT.NO.QAS SPINE SPINAL MOTION

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code MJO·June 14, 2019