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

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    Prismaflex ST60 Set, Prismaflex ST100 Set, Prismaflex ST150 set

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

    SIROSONIC

    FDA UDI
    SIRONA Dental Systems GmbH·E27662122160·SIROSONIC TL

    Dornier MedTech

    FDA UDI
    Dornier MedTech GmbH·04049958003981·600 Micron D Luer/SMA Ident Calibration Lightgu...

    NA

    FDA UDI
    Synthes GmbH·10886982152237·5.0MM LOCKING SCREW SLF-TPNG WITH T25 STARDRIVE...

    Fibula Plate PROlock

    FDA UDI
    I.T.S. GmbH·09120034302664·Fibula Plate PROlock, 6-Hole, Right

    NIROYAL BILIARY PREMOUNTED STENT SYSTEM

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

    U-RIGHT TD-3128 BLOOD PRESSURE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CERTAIN TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·September 21, 2020

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 16, 2023

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·June 12, 2018

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·August 15, 2011

    MIC* TJ FEEDING TUBE KIT 18 FR, 45CM (SURGICAL)

    FDA Adverse Event
    Malfunction ·KIMBERLY-CLARK HEALTH CARE·Product code KNT·October 30, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 9, 2013

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·February 15, 2019

    CERTAIN® TITANIUM LARGE HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·February 14, 2019

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·August 10, 2016

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 12, 2019

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·August 12, 2019

    TISSOMAT AND SPRAY SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - VIENNA·Product code FMF·June 29, 2012

    TISSOMAT AND SPRAY SET

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - VIENNA·Product code FMF·June 29, 2012