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

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    RAYDENT SW

    FDA 510(k)
    FDA Class 2 ·Dental

    Numen Coil Embolization System; NumenFR Detachment System

    FDA 510(k)
    FDA Class 2 ·Neurology

    AGILITY 10 STANDARD & SOFT 0.01IN. X 195CM, AGILITY 14 STANDARD & SOFT 0.014IN X 205CM & XL 350CM, AGILITY 16 STANDARD &

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 22, 2025

    S-ROM HEAD FEMORAL COCR 28+6

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD·Product code JDI·November 14, 2008

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 2, 2011

    GEMINI?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·July 18, 2013

    METASUL DUROM, COMPONENT FOR ACETABULUM, UNCEMENTED, 48/ 42, CODE H

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·July 24, 2023

    BD ALARIS PUMP MODULE SMARTSITE INFUSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·February 26, 2024