BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    DIGITAL IMAGING SYSTEM INTERFACE

    FDA 510(k)
    FDA Class 1 ·Radiology

    Pulmoguard

    FDA UDI
    S D I DIAGNOSTICS INC·B279S297953080·Pulmonary Function Test Filter

    RTVue XR OCT Avanti with AngioVue Software

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GRAFTCAGE ACX

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PECTUS SYSTEM CHANEY 13 TI PECTUS BAR

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·December 30, 2019

    COMPREHENSIVE REVERSE HUMERAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·August 7, 2018

    COMPREHENSIVE REVERSE HUMERAL TRAY WITH LOCKING RING 44MM +5MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·August 7, 2018

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code LWS·February 9, 2013

    SEGURA HEMISPHERE STONE RETRIEVAL BASKET

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FFL·January 7, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 23, 2014

    COMP RVS HMRL TI TRAY 44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·August 7, 2018

    PECTUS SYSTEM CHANEY 13" TI PECTUS BAR

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·December 30, 2019

    PECTUS SYSTEM CHANEY 13 TI PECTUS BAR

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·December 30, 2019