BEUDAMED
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    6 FR DL POWERPICC CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    N/A

    FDA UDI
    GEORGE TIEMANN & CO.·B58210509310·SCISSORS, SURGICAL TISSUE, DENTAL

    AMS SACRAL COLPOPEXY SLING, MODEL 72403501

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AU5 ULTRASOUND IMAGING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    MULTI-LINK RX PIXEL CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code MAF·April 3, 2008

    INTIMA-II Y 26GAX0.56IN MZPRN SLM NPVC

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·May 24, 2019

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·April 10, 2013

    HAKIM PROG VALVE, RT ANGLE RES. SEPARABLE

    FDA Adverse Event
    Injury ·CODMAN AND SHURTLEFF, INC.·Product code JXG·April 4, 2011

    ATLAS II HF CRT-D

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·May 27, 2008

    BIODESIGN URETHRAL SLING

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code FTM·July 29, 2013