BEUDAMED
    10 results · 34ms · Sources: EU EUDAMED, US FDA

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    SAMSUNG RAYPAX LONG TERM ARCHIVE

    FDA 510(k)
    FDA Class 1 ·Radiology

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    TEMPORARY TRANSVENOUS PACMKER. ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    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

    SYMBIA T-SERIES

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

    E. CAM COMPUTER [510(K) K992731]

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC.·Product code IYX·April 20, 2001

    REPLY

    FDA Adverse Event
    Death ·SORIN CRM S.R.L.·Product code NVZ·March 1, 2013

    SIGNATURE KNEE GUIDE - 42-422451

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·February 15, 2011

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014