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

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    GC FUJI TEMP

    FDA 510(k)
    FDA Class 2 ·Dental

    Bur PM2-70 80K diam EC Ø5.0x80 St

    FDA UDI
    Bien-Air Surgery SA·17630055519570·

    20 DEGREE PRISM LENS

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112434·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L101420120·10mm H x 14mm W x 20mm L XLIF Trial 12 degree L...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383556187·Gutta Percha Points is used to root canal filin...

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930710142000·Curette XL 14" #2

    SLIDESCAN

    FDA 510(k)
    FDA Class 2 ·Hematology

    MM-87 MOTOR-DRIVE MANIPULATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    HELIX-REVOLUTION ACP SYSTEM

    FDA Adverse Event
    Malfunction ·NUVASIVE, INC.·Product code KWQ·April 30, 2013

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·May 24, 2011

    CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·August 14, 2017

    CANTATA 2.8 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·November 17, 2017

    CANTATA 2.5 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·September 17, 2018

    CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·September 11, 2018

    CANTATA 2.5 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Injury ·COOK INC·Product code KRA·July 28, 2017

    CANTATA DUO 2.8 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·June 15, 2017

    CANTATA 2.5 SUPERSELECTIVE MICROCATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRA·May 30, 2018

    EQUINOXE COMPRESSION SCREW

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 27, 2025

    UNKNOWN NEXGEN FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 29, 2025