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

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    DMC SAPHENOUS VEIN DISTENTION SYSTEM (SVDS)

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040043981·Excavator DE

    Leksell Stereotactic System

    FDA UDI
    Elekta Instrument AB·07340048305174·ARC SLIDE LEFT

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282505806·TeWa PB-Type 3025: coated acupuncture needles ...

    TEWA

    FDA UDI
    asia-med GmbH·04251282512798·TeWa PB-Type 3025: coated acupuncture needles ...

    Sochi

    FDA UDI
    Altus Spine, LLC·00843210135410·Head Positioner

    PenEvac1®, MaxReveal ™ Diamond Crystal®

    FDA UDI
    I.C. MEDICAL, INC.·00817688024187·PenEvac1®-ST, MaxReveal ™ Diamond Crystal Blade...

    ALLIANCE LEFT HEART DELIVERY SYSTEM INTRODUCER, MODEL #407509

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ARTHROCARE CONTROLLER, ARTHROCARE CABLE, FOOTSWITCH, POWERCORD, PLASMA SCALPEL GS, TURBOVAC GS

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

    AISYS

    FDA Adverse Event
    Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 15, 2016

    HAL-MEM WITH LAH #00-0704-00, 200L bag

    FDA UDI
    Lonza Walkersville, Inc.·00840075400677·

    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

    LARGE NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·March 12, 2013

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·February 8, 2011

    MICROSTAAR INJECTOR CARTRIDGE

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL·Product code KYB·February 21, 2008

    UNKNOWN TROFIX TROCHANTERIC FIXATION PLATE

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