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

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    ONDEMAND3D

    FDA 510(k)
    FDA Class 2 ·Radiology

    RADCALC, MODEL V.4.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    URINE OPIATES (OPI) SCREEN FLEX REAGENT CARTRIDGE, CATALOG NO. DF 90A

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·September 11, 2017

    CARTRIDGE

    FDA Adverse Event
    Injury ·GAMBRO RENAL PRODUCTS S.A. DE C.V.·Product code FJK·July 8, 2015

    UNKNOWN SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 22, 2024

    UNKNOWN LINER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·February 10, 2015

    PLANMECA INTRA X-RAY

    FDA Adverse Event
    Malfunction ·PLANMECA USA·Product code EHD·April 16, 2013

    ENDOPATH** XCEL* BLADELESS TROCAR WITH STABILITY SLEEVE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·April 27, 2011

    PROSTIVA

    FDA Adverse Event
    Malfunction ·MPROC, VILLALBA·Product code KNS·July 7, 2008