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

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    AUTODELFIA NEONATAL IRT KIT, MODEL B005-112

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    GLOBAL SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER-FREE NON-VHLORINATED POLYMER COATED LATEX EXAMINATION GLOVES CONTAINS 100 MICROGRAMS OR LESS OF TOTAL WATER EXTRA

    FDA 510(k)
    FDA Class 1 ·General Hospital

    UNO QUICK-SET 60/6 SC1 MECA

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·May 14, 2025

    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

    V500, SAVINA AND VENTILATORS OF EVITA FAMILY

    FDA Adverse Event
    Other ·DRAGER MEDICAL GMBH·Product code CBK·February 18, 2011

    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

    2520274-2013-10151

    FDA Adverse Event
    Malfunction ·Product code KTT·February 28, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·February 24, 2011

    CONTOUR CURVED CUTTER STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·February 14, 2008

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

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·October 27, 2016