BEUDAMED
    26 results · 31ms · Sources: EU EUDAMED, US FDA

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    AMS SPECTRA CONCEALABLE PENILE PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    OVERWATCH

    FDA UDI
    SPINAL ELEMENTS·00840916134747·Vertical Grip Persuader

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694038812·2.0mm x 6mm Midface Screw

    OVERWATCH

    FDA UDI
    SPINAL ELEMENTS·00840916155551·VERTICAL GRIP PERSUADER

    LIFESHIELD ADDITIVE PIERCING PIN

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDICAL DEPOT POWER NEB 1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SYMBIA T-SERIES

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·September 20, 2013

    E.CAM, SYMBIA E, SYMBIA S, SYMBIA T SERIES

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·May 31, 2013

    ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HSB·May 18, 2018

    ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HSB·May 18, 2018

    SPINNING SPIROS® CLOSED MALE LUER, RED CAP

    FDA Adverse Event
    Malfunction ·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·November 4, 2025

    E.CAM, SYMBIA E, SYMBIA S, SYMBIA T SERIES

    FDA Adverse Event
    Injury ·SIMENS MEDICAL SOLUTIONS, USA, INC. MI GROUP·Product code KPS·August 3, 2012

    E.CAM, SYMBIA E

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·July 13, 2012

    E.CAM, SYMBIA E

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code KPS·May 16, 2013

    ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HSB·May 18, 2018

    E.COM, SYMBIA E

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code IYX·March 15, 2012

    E.CAM

    FDA Adverse Event
    Injury ·SIEMENS MEDICAL SOLUTIONS USA, INC. MI GROUP·Product code KPS·January 7, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

    ENDOPATH** ETS45

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 9, 2011

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·DISETRONIC MEDICAL SYSTEMS, INC.·Product code LZG·July 23, 2008