BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    BriefCase

    FDA 510(k)
    FDA Class 2 ·Radiology

    MICRODOT & MICRODOT XTRA

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BOVIE ICON VS GENERAL PURPOSE RF GENERATOR, MODEL: VS300

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

    BD NEXIVA DIFFUSICS 22G X1.00 IN

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·May 9, 2024

    P.F.C. FLUT TIB ROD 75X14MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·October 2, 2008

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·June 27, 2013

    UNICEL DXI 800 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·August 5, 2011

    BD NEXIVA DIFFUSICS 22G X 1.00 IN

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·June 3, 2024