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

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    1.5T and 3.0T 16 CH GE Shoulder Coils

    FDA 510(k)
    FDA Class 2 ·Radiology

    ENDOLIGHT

    FDA UDI
    Richard Wolf GmbH·04055207012956·LIGHT SOURCE LED 1.3 76W LED, low operating no...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690190653·Femoral Sizing Guide Bushing 3 deg

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482056301·Symmetry® Demarcator, Pitanguy Flap, Small

    Eargo SE

    FDA UDI
    Eargo, Inc.·00850010429588·Eargo Charging Cable + Adaptor

    Liberty SI

    FDA UDI
    Spinal Simplicity, LLC·M9432001620010·Guidewire, Trocar

    CONMED

    FDA UDI
    Conmed Corporation·30653405009744·Laparoscopic Electrode with a 3/32" pin connect...

    ROSTAM SCENTED AND UNSCENTED PLASTIC APPLICATOR TAMPONS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MODIFICATION TO RENASYS EZ PLUS NEGATIVE PRESSURE WOUND THERAPY

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

    SAFETRACE

    FDA Adverse Event
    Malfunction ·WYNDGATE TECHNOLOGIES / DIV GLOBAL MED TECHNOLOGIES, INC.·Product code MMH·February 28, 2001

    ANGSTROM MD SERIES TIERED THERAPY DEFIBRILLATOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·March 14, 2001

    MEDTRONIC

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code LGW·December 27, 2002

    TRIUMPH-1 PORT

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·March 8, 2001

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Injury ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·February 2, 2001

    UNIPROBE

    FDA Adverse Event
    Malfunction ·NELLCOR DE MEXICO, S.A. DE C.V.·Product code DQA·February 23, 2001

    HUMERAL HEAD/TISSUE

    FDA Adverse Event
    Other ·AMERICAN RED CROSS·Product code LMO·January 9, 2003

    SACH FOOT FOR MEN -LIGHTWEIGHT

    FDA Adverse Event
    Injury ·OTTO BOCK ORTHOPADISCHE INDUSTRIE, GMBH·Product code ISH·February 8, 2001

    SABRATEK HOMERUN

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·April 24, 2001

    SERIES TWENTY THOUSAND LEGACY

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQE·November 14, 2001

    MC10 PULSE OXIMETRY CABLE

    FDA Adverse Event
    Death ·NELLCOR DE MEXICO, S.A. DE C.V.·Product code DQA·June 15, 2001