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

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    FUTURA SAFETY SYRINGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    RL-500

    FDA UDI
    DAESUNG MAREF CO.,LTD.·08809315679817·Hose 1ea, Com cable 1ea (1 set box)

    PowerMidline

    FDA UDI
    Bard Access Systems, Inc.·00801741162763·Catheter Placement Kit

    Thermoflect

    FDA UDI
    Encompass Group, L.L.C.·00612899005907·THERMOFLECT GOWN KIT, 25 EA ...

    ZENTRUM 100 CM CARBON FIBER EXTENSION

    FDA UDI
    MIZUHO ORTHOPEDIC SYSTEMS, INC.·00842430104077·

    Cervical Plate

    FDA UDI
    Eisertech, LLC·B5231000860·Lock cover for Cervical Plate

    PedFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361008163·PedFuse ReTurn, Hex, CNL, 8.0mm x 60mm

    GEL MARK BIOPSY SITE MARKER, MODELS MKOOO1, MK0004, MK0007

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

    RX G-UNIVERSAL

    FDA 510(k)
    FDA Class 2 ·Dental

    BARD POWERMIDLINE CATHETER 3F, SINGLE-LUMEN

    FDA Adverse Event
    Malfunction ·Product code PND·October 5, 2021

    PATIENT INFORMATION CENTER IX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·November 13, 2024

    CARDIOSAVE HYBRID, TYPE B PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·June 6, 2025

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 27, 2023

    CS300

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP·Product code DSP·July 2, 2014

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 110V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·December 12, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 13, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION VALENCIA·Product code LGW·February 17, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·February 21, 2008

    CARDIOSAVE HYBRID TYPE D PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·September 18, 2023

    CARDIOSAVE HYBRID, TYPE G PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 1, 2022