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

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    Velano Vascular Blood Collection Adapter

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    10PW - Penn Power & Light

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588012179·10PW - Penn Power & Light

    PHOENIX SFS

    FDA UDI
    Orthofix US LLC·18257200134410·7.5MM CANULATED JANUS TAP

    PYRAMID PLUS (6 HOLE)

    FDA UDI
    The Wells Johnson Company·B458201237000·Cannula, Pyramid Plus, specify length, diameter...

    COOPERSURGICAL LAPAROSCOPIC INSTRUMENTS

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

    EQUINOX OCCLUSION BALLOON CATHETER/SYSTEM - (10MM BALLOON, 4 & 13 MM TIP), (15 MM BALLOON, 4 & 13 MM TIP), (20 MM BALLOO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EVIS LUCERA ELITE DUODENOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDT·November 30, 2023

    2520274-2013-06518

    FDA Adverse Event
    Injury ·SYNTHES, USA·Product code HWC·September 25, 2013

    ARTHREX MINI BIO-SUTURE TAK SUTURE ANCHOR

    FDA Adverse Event
    Injury ·ARTHREX·Product code MAI·August 12, 2023

    2520274-2013-06522

    FDA Adverse Event
    Injury ·SYNTHES, USA·Product code HRS·September 25, 2013

    2530088-2013-01203

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·September 30, 2013

    2520274-2013-06607

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·September 30, 2013

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·October 27, 2014

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·July 29, 2011

    SPEEDBAND SUPERVIEW SUPER 7?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code MND·July 2, 2013

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·March 1, 2012