BEUDAMED
    27 results · 29ms · Sources: EU EUDAMED, US FDA

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    IMMULITE 2000 FREE PSA CALIBRATION VERIFICATION MATERIAL

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814749·GENUMEDI EXTRA WIDE SAND SIZE VI

    Oticon

    FDA UDI
    Oticon A/S·05707131264671·RIA PRO, KIT 312 DIR 85 R V BE

    COHESION BONE CEMENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHES (USA) MODIFICATION TO STERNAL RECONSTRUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PERIPHERAL NERVE BLOCK SUPPORT TRAY

    FDA Adverse Event
    Malfunction ·I-FLOW, LLC·Product code CAZ·October 1, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 1, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 29, 2013

    12MM SILS PORT

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL·Product code GCJ·May 12, 2011

    CONTINUOUS TRAY WITH 100MM NEEDLE, STIMULATING

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code CAZ·October 2, 2014

    CONTINUOUS TRAY WITH 100MM NEEDLE 4IN ECHO NEE

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code CAZ·October 3, 2014

    CONTINUOUS TRAY WITH 100MM NEEDLE, NON STIMULA

    FDA Adverse Event
    Malfunction ·I-FLOW LLC·Product code CAZ·October 1, 2014

    PERIPHERAL NERVE BLOCK SUPPORT TRAY : CONTINUEOUS TRAY 100MM NEEDLE STIMULATING

    FDA Adverse Event
    Malfunction ·HALYARD - IRVINE·Product code CAZ·May 12, 2015

    CONTINUOUS TRAY WITH 100MM NEEDLE STIMULATING & 61CM CATHETER

    FDA Adverse Event
    Malfunction ·HALYARD HEALTH - IRVINE·Product code CAZ·November 8, 2015

    CONTINUOUS TRAY WITH 100MM NEEDLE STIMULATING

    FDA Adverse Event
    Malfunction ·HALYARD - IRVINE·Product code CAZ·July 1, 2015

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·June 3, 2024

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER (ISRAEL) LTD.·Product code DQK·December 22, 2016