BEUDAMED
    83 results · 28ms · Sources: EU EUDAMED, US FDA

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    1688 Pendulum 4K Camera Head with Integrated Coupler, 1688 4K Camera Control Unit with Advanced Imaging Modality

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

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517184405·MaXcess Access Driver, Solid

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694011037·1.3mm Pilot Drill, OSTEOPOWER

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694015042·1.6mm Pilot Drill, Calibrated, Short Pointed Ca...

    COTTLE-DORSAL SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896083622·COTTLE-DORSAL SCISSORS HEAVY BLADE POWER CUT GOLD

    Accufit

    FDA UDI
    Ortho Organizers, Inc.·00190707183523·Accufit Molar Bands Lower Left First Molar 31

    PTS Transport Bag

    FDA UDI
    Delfi Medical Innovations Inc·M995922003101·Delfi’s PTS Transport Bag and Transport Case ar...

    WALKAIDE SYSTEM, MODELS 20-0100, 20-0310, 20-1000

    FDA 510(k)
    FDA Class 2 ·Neurology

    DAVLITE MICROENDOSCOPE & ACCESSORIES

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

    VOYAGER 6.0 SOFTWARE OPTION

    FDA 510(k)
    FDA Class 2 ·Neurology

    UCR SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·SEASPINE, INC.·Product code KWP·February 5, 2004

    NEW CORONA VIRUS NUCLEIC ACID DETECTION KIT

    FDA Adverse Event
    Malfunction ·PERKINELMER, INC.·Product code QJR·March 5, 2021

    APEX MODULAR HIP STEM

    FDA Adverse Event
    Injury ·OMNI LIFE SCIENCE INC.·Product code KWY·June 30, 2008

    INTERGARD KNITTED ULTRATHIN SILVER VASCULAR PROSTHESIS

    FDA Adverse Event
    INTERVASCULAR·Product code DSY·July 4, 2003

    APEX MODULAR HIP STEM

    FDA Adverse Event
    Injury ·OMNI LIFESCIENCE, INC.·Product code KWY·July 15, 2009

    APEX MODULAR HIP STEM

    FDA Adverse Event
    Injury ·OMNI LIFE SCIENCE, INC·Product code KWY·November 27, 2006

    T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OZO·October 10, 2019

    APEX MODULAR HIP STEM

    FDA Adverse Event
    Injury ·OMNI LIFE SCIENCE, INC.·Product code JDI·February 19, 2007

    LUMBAR SCREW 6.7 X 40 MM + BALL RING

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code HWC·June 15, 2006

    CLINAC

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC.·Product code IYE·August 19, 2003