BEUDAMED
    241 results · 24ms · Sources: EU EUDAMED, US FDA

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    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·ConMed PadPro Multifunction Electrodes, ConMed PadPro Multifunction Electrode Adapters

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·ConMed PadPro Multifunction Electrodes

    PADPRO:AD;RTRANS EL/LW, 12X7

    FDA Adverse Event
    Injury ·KATECHO, INC.·Product code MKJ·October 7, 2022

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377045270·RELINE-O Trial, 8mm H Lamina N L-pop

    Paradigm

    FDA UDI
    Proprio, Inc.·00850042604069·Paradigm Straight Pedicle Probe

    JEWELERS FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084407·JEWELERS FORCEPS STRAIGHT TUNGSTEN CARBIDE DUST...

    Scalpel

    FDA UDI
    Treace Medical Concepts, Inc.·00810111222501·Scalpel

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694005586·1.6mm Pilot Drill, Long, J-Latch

    OptumSI Implant System

    FDA UDI
    SI Solutions, LLC·00850057247046·Broach

    Treace Medical Concepts

    FDA UDI
    Provision·B504OM02000040·

    Clarius Ultrasound Scanner

    FDA UDI
    Clarius Mobile Health Corp·07540205000014·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694066167·2.0 System 16mm Pilot Drill Long J-Latch Steril...

    COMPRESSURE FRACTURE REPAIR IMPLANT

    FDA Adverse Event
    Injury ·USI ORTHOPAEDICS LLC DBA U.S. ORTHOPAEDICS·Product code HTN·April 6, 2011

    AGILIA SP MC WIFI CA

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S·Product code FRN·May 23, 2024

    AGILIA SP MC WIFI CA

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S·Product code FRN·May 23, 2024

    ARTHROCARE CONTROLLER, MODEL H2000; ARTHROCARE CABLE, MODEL H0970-02; FOOTSWITCH, MODEL H2000-04; POWERCORD, MODEL H2000

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

    ARTHROCARE CONTROLLER, CABLE, FOOT CONTROL, POWER CORD, WANDS, MODELS H0970-02, H2000-04, H2000-05, H0970-06

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

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 10, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Death ·ABBOTT VASCULAR - REDWOOD CITY·Product code MGB·October 16, 2008

    ENDO ILS 21MM, CURVED

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 1, 2013