BEUDAMED
    13 results · 19ms · Sources: EU EUDAMED, US FDA

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    EXCEL PULSED IRRIGATION/SUCTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Pads

    FDA UDI
    Baxter Medical Systems GmbH + Co. KG·00887761969421·Pad TTS Carbon one part B

    Trumpf Medical

    FDA UDI
    Baxter Medical Systems GmbH + Co. KG·00887761995994·Hospital Device

    MALLINCKRODT

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code BTR·August 16, 2012

    Panthera Dental Milled Bars

    FDA 510(k)
    FDA Class 2 ·Dental

    SMITH & NEPHEW INTRADISCAL CATHETER SYSTEM

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

    VNGD SSK 360 R FEM 60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·April 10, 2019

    BMT SPLINED KNEE STM V2 12X120

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·April 9, 2019

    MALLINKRODT

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY TYCOHEALTHCARE·Product code JOH·August 17, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2014

    PATIENT SPECIFIC CUTTING GUIDE - TRIATHLON RIGHT-

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS ALAMEDA·Product code MBH·November 15, 2012

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 20, 2010

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024