BEUDAMED
    16 results · 21ms · Sources: EU EUDAMED, US FDA

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    Visalys Core, Visalys PL-Core, Visalys PL-Core-C, Visalys PL-Core-X

    FDA 510(k)
    FDA Class 2 ·Dental

    E+R,Ever Ready First Aid

    FDA UDI
    Wenzhou Caretek Medical Device Co., Ltd.·06975871430239·SINGLE HEAD STETHOSCOPE GREEN

    MAXIM® VI KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00887868225802·

    MAXIM VI KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304205734·

    SPECIAL ORTHOPAEDIC SOLUTIONS GLENOID SHOULDER COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KODAK ORTHODONTIC IMAGING AND OMS IMAGING 8.0

    FDA 510(k)
    FDA Class 2 ·Dental

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971406·

    WAVEWRITER ALPHA PRIME 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 30, 2024

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 6, 2025

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·May 20, 2016

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·March 17, 2015

    PARIETEX UGYTEX PP POSTERIOR KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTP·May 24, 2013

    EON RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 23, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    RIGID ARM SUPPORT, STANDARD AND LARGE

    FDA Adverse Event
    Malfunction ·MEDTEC, INC. D/B/A CIVCO MEDICAL SOLUTIONS·Product code IYE·July 28, 2017

    Roche/Hitachi Modular Additional D Module DAT clinical chemistry analyzer; catalog number 04429389160.

    FDA Recall
    Terminated ·Roche Diagnostics Corp.·Product code JJE·August 6, 2004