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

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    X-BOLT Hip Fracture Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1816400·18mm H x 16mm W x 40mm L x 0 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L181640120·18mm H x 16mm W x 40mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X181640120·18mm H x 16mm W x 40mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X18164080·18mm H x 16mm W x 40mm L x 8 degrees XLIF

    Regatta

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158606·Lateral Implant, 18mm x 16mm x 40mm, 10 Deg

    Regatta

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158590·Lateral Implant, 18mm x 16mm x 40mm,0 Deg

    PRECISION FLOW(R) - HELIOX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS

    FDA 510(k)
    FDA Class 2 ·Neurology

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·August 25, 2017

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD EAST) PHARMACEUTICAL SYSTEMS·Product code GAA·July 28, 2017

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 14, 2017

    19 G BD¿ 5 MICRON FILTER NEEDLE 1 1/2 IN., STERILE, SINGLE USE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·July 23, 2017

    19 G X 1 1/2 IN. BD NOKOR¿ FILTER NEEDLE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code GAA·August 18, 2017

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 8, 2017

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SWINFORD·Product code KDI·June 21, 2013

    ECHELON 60

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 27, 2011

    ULTRASOFT LACING DEVICE

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code FMK·September 29, 2008

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·October 10, 2017

    PENUMBRA SYSTEM REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·March 4, 2022