BEUDAMED
    14 results · 28ms · Sources: EU EUDAMED, US FDA

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    BACT/ALERT BLOOD COLLECTION ADAPTER CAP AND INSERT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981151775·Ventura NM Trial, 11mm x 24mm x 14mm

    MODIFIED DISTAL RADIUS PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLOSENSE II, MODEL 29-8040

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    WALLFLEX ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·January 16, 2025

    ANEURX - UNK

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·August 16, 2017

    WALLFLEX ESOPHAGEAL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·January 23, 2025

    WALLFLEX ESOPHAGEAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·February 14, 2025

    DELTAPAQ - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·January 29, 2013

    BILIARY STENT, BILIARY STENT SYSTEM, BILIARY ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·December 21, 2010

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ITJ·July 15, 2014

    LINER 10 DEGREE 36 MM I.D. SIZE F

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·December 22, 2020

    WALLFLEX ESOPHAGEAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code ESW·May 28, 2025

    LINER 10 DEGREE 36 MM I.D. SIZE F

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·December 22, 2020