BEUDAMED
    17 results · 28ms · Sources: EU EUDAMED, US FDA

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    MYOTEST DBS NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    THE BIONIC EXERCISER

    FDA 510(k)
    FDA Class 2 ·Neurology

    UNIFOCAL VP, MODELS 7501 AND 7502

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Injury ·AESCULAP INC·Product code KCT·October 12, 2016

    IOCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 3, 2014

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·November 1, 2010

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·December 31, 2012

    NAVITOR TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Death ·ABBOTT MEDICAL·Product code NPT·October 17, 2023

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code KCT·July 26, 2016

    FLEXNAV DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code NPT·October 17, 2023

    TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420578

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021

    TRUMATCH CT FEM CUT TIB PIN R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420907

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021

    TRUMATCH CT PIN GUIDE KIT R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420579

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021

    TRUMATCH CT PIN GUIDE FEM R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420581

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021

    TRUMATCH CT CUT GUIDE KIT R- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420916

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021

    TRUMATCH CT CUT GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420915

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021

    TRUMATCH CT CUT GUIDE FEM L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical instrumentation to assist in the positioning of a joint replacement component intra-operatively and in guiding the marking of bone before cutting Part Number: 420917

    FDA Recall
    Terminated ·DePuy Orthopaedics, Inc.·Product code NJL·August 10, 2021