BEUDAMED
    23 results · 32ms · Sources: EU EUDAMED, US FDA

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    Anatomical Shoulder Domelock Dome centric

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1616200·16mm H x 16mm W x 20mm L x 0 degrees XLIF

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528102220·4.5/5.5 mm Headless Compression Screw Reduction...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311616200·

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321616200·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X16162080·16mm H x 16mm W x 20mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X161620120·16mm H x 16mm W x 20mm L x 12 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L161620120·16mm H x 16mm W x 20mm L XLIF Trial 12 degree L...

    SKELETAL DYNAMICS GEMINUS VOLAR DISTAL RADIUS PLATE MODEL STANDARD 3 HOLE RIGHT, STANDARD 3 HOLE LEFT, SKELETAL DYNAMICS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    IFS CANNULATED BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·May 20, 2014

    PENUMBRA SYSTEM ACE 68 REPERFUSION CATHETER

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

    PENUMBRA SYSTEM ACE 68 HI-FLOW KIT

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

    VITALITY 2

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 14, 2011

    ESSURE

    FDA Adverse Event
    Injury ·CONCEPTUS·Product code HHS·June 4, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2014

    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

    TPRLC 133 T1 PPS SO 16X152MM T1

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·July 21, 2022

    PENUMBRA SYSTEM REPERFUSION CATHETER

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