BEUDAMED
    27 results · 24ms · Sources: EU EUDAMED, US FDA

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    Neuro.Al Algorithm

    FDA 510(k)
    FDA Class 2 ·Radiology

    Colorbite D

    FDA UDI
    ZHERMACK SPA·EZHIC2007501·Addition silicone for Bite Registration

    Pantheon PFR System

    FDA UDI
    ADLER ORTHO SPA·08050880237951·Pantheon Salvage Plate with Spikes Compression ...

    METZENBAUM SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055582·METZENBAUM SCISSORS STRAIGHT TENOTOMY TIP BLADE...

    McINDOE DRESSING/TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896061286·McINDOE DRESSING/TISSUE FORCEPS FINE SERRATIONS

    RHIGENE MESACUP2 TEST- SCL-70

    FDA 510(k)
    FDA Class 2 ·Immunology

    DIGITAL ELECTRICAL MUSCLE STIMULATOR, MODEL EV-807 DIGITAL EMS

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    INTRATHECAL CATHETER

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·March 26, 2008

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    COAGUCHEK XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·March 9, 2009

    GYNECARE MESH UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTM·August 3, 2018

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·August 1, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·August 1, 2018

    ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAT·August 1, 2018

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·October 24, 2014

    TM MONOBLOCK PATELLA

    FDA Adverse Event
    Injury ·ZIMMER TMT·Product code JWH·July 26, 2011

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code LHI·July 1, 2013

    PATIENT INTERFACE NIM4CPB1 NIM 4.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 28, 2025

    MINIMED 770G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 19, 2021

    ASCENDA

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code LKK·December 14, 2015