BEUDAMED
    601 results · 25ms · Sources: EU EUDAMED, US FDA

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    STERRAD NX Sterilizer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613088026·Instrument Guards, Clear, 1/15" x 3/8" x 1

    Avalign

    FDA UDI
    Avalign Technologies, Inc.·00190776020965·Keyhole Bracket

    II Ring Retractor

    FDA UDI
    Automated Medical Products Corp.·00810118342431·St. Mark’s Retractor 7" with Lip

    DMS 300-7

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376667720·12mm CORE, NANOTEC BAN 16 x 20 mm 7°

    Ascend

    FDA UDI
    ALPHATEC SPINE, INC.·00190376668130·12mm CORE, NANOTEC KBN 16 x 20 mm 7°

    SOMATOM EMOTION 16 (2007)

    FDA Adverse Event
    Injury ·SIEMENS SHANGHAI, MEDICAL EQUIPMENT LTD.·Product code JAK·July 5, 2023

    SOMATOM EMOTION 16 (2007)

    FDA Adverse Event
    Injury ·SIEMENS HEALTHCARE GMBH·Product code JAK·September 9, 2019

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC./ HUNTINGTON·Product code HQL·August 30, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code HQL·August 30, 2007

    ACCURUS HIGH BRIGHTNESS ILLUMINATOR

    FDA Adverse Event
    Malfunction ·ALCON PRECISION DEVICE - SINKING SPRING·Product code MPA·May 16, 2007

    SWEDISH ADJUSTABLE GASTRIC BAND

    FDA Adverse Event
    Injury ·OBTECH MEDICAL SARL·Product code LTI·November 16, 2007

    CONTOUR CURVED CUTTER STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GDW·April 17, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORTORIES, INC./ HUNTINGTON·Product code HQL·May 9, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON LABORATORIES, INC. HUNTINGTON·Product code HQL·May 9, 2007

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 3, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 24, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·July 11, 2011