BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    Aplio i900/i800/i700 Diagnostic Ultrasound System, V2.1

    FDA 510(k)
    FDA Class 2 ·Radiology

    Mouthpiece, Disposable, 1.045" O.D., 2.625" L

    FDA UDI
    A-M SYSTEMS, LLC·00817081024135·Mouthpiece, Disposable, 1.045" O.D., 2.625" L

    Biomet® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868310805·

    BIOMET HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304256798·

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111402142·SIMS TC UTER SCISS 9 INCHESSTR BL/BL

    SILEX SACROILIAC JOINT FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FOTONA XP ND: YAG LASER SYSTEM

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

    WAVEWRITER ALPHA? 16

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·January 16, 2026

    KANGAROO

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·October 16, 2024

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 11, 2013

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Other ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 16, 2011

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 9, 2008

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·March 15, 2023

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Death ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 9, 2023