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

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    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065852·EXTRAORAL ELASTICS 1/2" 8 oz

    GAMBRO WATER PURIFICATION UNIT, MODELS WRO 300 AND WRO 300 H

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

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065821·EXTRAORAL ELASTICS 1/4" 8 oz

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065814·EXTRAORAL ELASTICS 3/16" 8 oz

    SOVEREIGN BIPOLAR INSTRUMENTS FOR GYNECOLOGY

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DIGITAL RADIOGRAPHY SYSTEM, MODEL DFP-8000D

    FDA 510(k)
    FDA Class 2 ·Radiology

    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

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 21, 2025

    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

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Death ·MPRI·Product code DTB·May 6, 2013

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 4, 2014