BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    TENS device-HeadaTerm, eEspress

    FDA 510(k)
    FDA Class 2 ·Neurology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169596139·TRIAL 2172450 O25 IB 20MM 12 DEG 14X50

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741724500·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027359·2.4mm X 50mm Cannulated Headless Screw

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674172450060·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694069182·Cannulated 2.4 x 50mm Headless Screw Sterile Qty 2

    IONOLUX PRO

    FDA 510(k)
    FDA Class 2 ·Dental

    ESPRIT VENTILATOR AUTO-TRAK SENSITIVITY OPTION, MODEL V1000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HEARTMATE 3 VAD MODULAR CABLE

    FDA Adverse Event
    Malfunction ·THORATEC CORPORATION·Product code DSQ·September 26, 2023

    DELTA CERAMIC FEM HD 36/-3MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·March 28, 2018

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 17, 2013

    CCU BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 17, 2011

    ANALYTICAL P MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·September 19, 2008

    4.5MM VA-LCP CURVED CONDYLAR PLATE/20HOLE/405MM/RT-STER

    FDA Adverse Event
    Injury ·OBERDORF : SYNTHES PRODUKTIONS GMBH·Product code JDP·November 30, 2017

    BD ALARIS SMARTSITE EXTENSION SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·May 6, 2022