BEUDAMED
    23 results · 21ms · Sources: EU EUDAMED, US FDA

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    WV3000T DIGITAL X-RAY DIRECT IMAGING FLAT PANEL DETECTOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    EVOTECH™

    FDA UDI
    ADVANCED STERILIZATION PRODUCTS SERVICES INC.·10705037067206·Connector Tube, Orange and Brown

    ACEMST1

    FDA UDI
    ACEM SPA·08050705890057·ACEMST1.1 ARTICULATED ARM TABLE

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306803611·Light pipe only for breast retractors, size: 100mm

    Aurora Spine

    FDA UDI
    AURORA SPINE, INC.·B5211108010·ANTERIOR DISK PREP, INSTRUMENT SET

    Matira

    FDA UDI
    Kalitec Direct LLC·B07307K1100010·Tray Insert 1, Matira, Arcamed

    n/a

    FDA UDI
    Ortho Development Corporation·00822409066711·Stem Extension Trial Diameter 11x80mm

    n/a

    FDA UDI
    Ortho Development Corporation·00822409070206·Snap-on Fem Augment Trial 8mm Distal Size 1

    PUMA MODEL VERSION 1.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    T2 FEMORAL NAIL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DONJOY

    FDA UDI
    DJO, LLC·00888912003933·COLD PAD,UNIV,FOAM,S,RH

    BD¿ NSYTE AUTOGUARD SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·December 21, 2018

    UNSPECIFIED BD¿ PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·May 20, 2023

    UNSPECIFIED BD¿ PEN NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·May 20, 2023

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 3, 2018

    BD INSYTE¿ AUTOGUARD¿ SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·June 11, 2018

    ULTRASONIC IMAGING CATHETER - CORONARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code DQO·May 14, 2013

    ARTICUL/EZE BALL 32 +5 BR

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code JDI·September 23, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 1, 2011

    HANDLE CEV669B DIA 5MM ANG BIPOLAR [MXI/XOM]

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INSTRUMENTATION S.A.S·Product code GEI·July 31, 2013