BEUDAMED
    22 results · 24ms · Sources: EU EUDAMED, US FDA

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    FastFrame External Fixation System - Knee Spanning, FastFrame External Fixation System - Damage Control

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3D SCANNER, MODEL 1230

    FDA 510(k)
    FDA Class 2 ·Radiology

    POWERED PD-IO INTRAOSSEOUS INFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CD SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SOFAMOR DANEK EUROPE·Product code KWQ·September 3, 1999

    VARIABLE ANGLE SCREW

    FDA Adverse Event
    Injury ·SOFAMOR DANEK MANUFACTURING·Product code KWP·December 3, 1998

    INFLATABLE PENILE PROSTHESIS

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS·Product code FAE·July 22, 1993

    FAULTLESS DELUXE WATER BOTTLE

    FDA Adverse Event
    Injury ·ROSS LABORATORIES·Product code FPF·August 25, 1992

    RECTAL THERMOMETER

    FDA Adverse Event
    Injury ·IVAC·Product code EXX·June 30, 1992

    TISSUE EXPANDER

    FDA Adverse Event
    Malfunction ·MCGHUN CUSTOM·April 27, 1993

    ANGIOCATH (22GA 1")

    FDA Adverse Event
    Malfunction ·BECTON/DICKINSON·Product code FOZ·June 9, 1992

    POLARIS DUAL CENTER

    FDA Adverse Event
    Malfunction ·AMSCO COMPANY·Product code FTD·August 11, 1993

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 8, 2014

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·June 7, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

    RELOADER STAPLER UNIT

    FDA Adverse Event
    ETHICON, INC.·Product code GAG·July 2, 1992

    ST. JUDE MEDICAL PROSTHETIC HEART VALVE/AORTIC EXPANDED-

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code LWQ·March 15, 1993

    NONE

    FDA Adverse Event
    Death ·ACMI·Product code MCJ·May 12, 1992

    ARTHROSCOPE

    FDA Adverse Event
    Injury ·KARL STORZ·Product code HRX·October 22, 1992

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FZW·November 22, 2013

    OLYMPUS OES BRONCHOFIBERSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code EOQ·March 18, 2010