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

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    DIRECT TIBC KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PowerPICC

    FDA UDI
    Bard Access Systems, Inc.·00801741143861·Catheter Placement Kit

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040044025·Elevator Root Tip #80

    TruLock

    FDA UDI
    Rmo, Inc.·00885797644893·TRULOCK Light Activated Adhesive Kit (40 Capsule)

    Medallion®

    FDA UDI
    Merit Medical Systems, Inc.·00884450096154·

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·August 15, 2024

    MANUAL AND REMOTE CONTROLLED APPLICATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    HARDYDISK, CARBENICILLIN, 100MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    ENVISTA INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code HQL·April 15, 2015

    CARDIOSAVE HYBRID, TYPE I PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DSP·March 5, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·February 27, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 16, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 10, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·February 27, 2025

    0.25MM SLOTTED SCREWDRIVER BLDHEX COUPLING

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HXX·March 12, 2013

    HAKIM PROGRAMMABLE VALVE WITH PRECHAMBER

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC, MEDOS S.A.·Product code JXG·February 16, 2011

    HEARTSTART MRX-EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·February 21, 2008