BEUDAMED
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    MICROLIFE DIGITAL INFRARED EAR THERMOMETER, IR1DAI, IR1DB1, IR1DD1

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·10304040134594·Engine Files 21mm

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·H65810033081·ENGINE FILES 21MM

    ADVANCE®

    FDA UDI
    Microport Orthopedics Inc.·M684K00533081·

    3M™ Unitek™ APC™ Clarity™ MBT™

    FDA UDI
    3M UNITEK CORPORATION·00652221236913·APC FF Clarity Ultra SL MBT U Rt Cuspid 0T/8A D...

    MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    WALLSTENT BILIARY ENDOPROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·July 21, 2016

    JAW INS.BIP.MACRO FORCEPS D: 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG TUTTLINGEN 78532·Product code GEI·December 12, 2014

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    JAW INS. BIP. MARYLAND DISS. FCPS 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·January 14, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·October 25, 2016

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·May 10, 2016

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013

    INFUSOMAT SPACE - US VERSION

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·July 31, 2014