BEUDAMED
    13 results · 23ms · Sources: EU EUDAMED, US FDA

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    FUJIFILM Endoscope Model EG-740N

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331161315·tuttle (singley) tissue forceps, 10" (25.0 cm)

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    ICU MEDICAL UNIVERSAL SINGLE-USE SPIKES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BONASIL A+ IMPRESSION MATERIALS

    FDA 510(k)
    FDA Class 2 ·Dental

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·January 20, 2025

    TARGET DEVICE 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·March 2, 2012

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 9, 2022

    APOLLO SYSTEM APOLLO WAND

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code GWG·October 17, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·June 11, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 8, 2011

    MUSTMINI OCCIPITAL SCREW

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code NKG·February 11, 2025

    MUST MINI OC PRE-BENT TRANSITION ROD 75° Ø3.5/4X 200MM (STE)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKG·April 25, 2024