BEUDAMED
    20 results · 24ms · Sources: EU EUDAMED, US FDA

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    KSEA GAAB NEUROENDOSCOPE AND CHAVANTES-ZAAMORANO NEUROENDOSCOPE SETS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Walgreens

    FDA UDI
    WALGREEN CO.·00311917191898·WAG Walker/Commode Tips 1-1/8"

    M.U.S.T. Mini Extension

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STERILE FIELD SALINE PRE-FILLED SYRINGE(S)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MUSTMINI OCCIPITAL SCREW

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

    CADD LEGACY PLUS PUMP

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

    CADD LEGACY PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·April 11, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 8, 2022

    CADD LEGACY PLUS PUMP

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

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 23, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 22, 2022

    POSEY KEEPSAFE DELUXE

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·January 31, 2013

    CE INFUSOR LV 5, 12 PACK

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·February 9, 2011

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 22, 2022

    CADD LEGACY PLUS PUMP

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·September 8, 2022

    CADD LEGACY PLUS PUMPS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·October 29, 2022

    CADD LEGACY PLUS PUMPS

    FDA Adverse Event
    Malfunction ·ST PAUL·Product code FRN·October 24, 2022

    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