BEUDAMED
    29 results · 25ms · Sources: EU EUDAMED, US FDA

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    QUANTA LITE ASCA (S. CEREVISIAE) IGA ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    Bard Jejunal Feeding/Gastric Decompression Tube

    FDA UDI
    Bard Access Systems, Inc.·00801741051678·12 Fr Tether J-Tube

    GENESIS I

    FDA UDI
    Smith & Nephew, Inc.·00885556914069·GENESIS ARTICULAR INSERT MEDIUM ...

    Genesis I

    FDA UDI
    Smith & Nephew, Inc.·00885556915202·GENESIS ARTICULAR INSERT MEDIUM ...

    GENESIS I

    FDA UDI
    Smith & Nephew, Inc.·00885556914076·GENESIS ARTICULAR INSERT LARGE ...

    Genesis I

    FDA UDI
    Smith & Nephew, Inc.·00885556915219·GENESIS ARTICULAR INSERT LARGE ...

    FlowLogic Assert

    FDA UDI
    SONENDO, INC.·00810209420468·FlowLogic Assert Shaping File 10/.06, 25mm

    MENICON Z

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MENICON SF-P

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Trulink

    FDA UDI
    SPACELABS HEALTHCARE (WASHINGTON), INC·10841522122804·LDWR SET,V LDS,SNAP,ECG,127CM/50IN,5LW/SET,BX/25

    Endo Carry-On Procedure Kit

    FDA UDI
    MEDIVATORS INC.·00677964106286·Endo Carry-On Procedure Kit

    UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code KTT·August 22, 2023

    UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code KTT·August 22, 2023

    UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KTT·August 22, 2023

    UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KTT·August 14, 2023

    UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURER GMBH·Product code KTT·August 22, 2023

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    LERADO GLOBAL·Product code ILS·March 12, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·February 16, 2011

    DIMENSION CLINICAL CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSITICS INC.·Product code MMI·February 19, 2008

    4F M-I STIFFEN 40CM NT-SS (610366)

    FDA Adverse Event
    Malfunction ·GALT MEDICAL CORP.·Product code DQX·January 10, 2012