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

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    CORMATRIX PROTECT ECM ENVELOPE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699588·GENUMEDI PSS BLUE, SIZE VI

    INTREPED, Intraosseous Fusion Device

    FDA UDI
    Auxano Medical LLC·00850055649187·INTREPED 06 Sizer

    ADSON TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896023536·ADSON TISSUE FORCEPS WITH TUNGSTEN CARBIDE SERR...

    KENDALL SCD SEQUENTIAL COMPRESSION COMFORT SLEEVES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    T:SLIM X2, BASAL-IQ, MMOL/L

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·May 29, 2020

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·November 1, 2023

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 12, 2024

    LOGIC FEMORAL PS POR RIGHT SZ 2

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·February 10, 2025

    CATHETER MOUNT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZO·September 2, 2014

    UNKNOWN_LIM_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·October 3, 2014

    HICKMAN 12 FR DUAL-LUMEN CV CATHETER, PEEL-APART INTRODUCE

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·May 24, 2013

    DUET TRS 60 4.8MM ARTICULATING SULU

    FDA Adverse Event
    Injury ·UNITED STATES SURGICAL·Product code GDW·June 15, 2011

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 9, 2023

    BI-LEVEL/CPAP INSPIRATORY HEATED CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·August 6, 2014

    LOGIC CR FEMORAL POR, LEFT, SZ 3.5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·December 11, 2024

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 5, 2023

    VASERLIPO SYSTEM

    FDA Adverse Event
    Injury ·SOLTA MEDICAL, INC·Product code QPB·January 10, 2023

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 26, 2023