BEUDAMED
    31 results · 25ms · Sources: EU EUDAMED, US FDA

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    NuVasive Navigation.S Instruments

    FDA 510(k)
    FDA Class 2 ·Neurology

    N/A

    FDA UDI
    STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825003609·Diagnostic EP Catheter, Damato curve, 4 electro...

    CONVERSE WILMER SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055537·CONVERSE WILMER SCISSORS SERRATED BLADES POWER ...

    LFI-DOWN RETRACTOR

    FDA UDI
    W.H. Holden, Inc.·D9282007190·

    NEOCARE 20 MICRON BLOOD FILTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SURGASSIST SYSTEM STRAIGHT LINEAR CUTTER DIGITAL LOADING UNIT, 55MM, 30MM WITH BLUE AND GREEN RELOAD CARTRIDGES

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

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·November 7, 2007

    DEEP BRAIN STIMULATION LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·November 7, 2007

    PEN NDL 32G 6MM 3B TW 100CT US

    FDA Adverse Event
    Malfunction ·EMBECTA PENEL LIMITED - DUN LAOGHAIRE, IRELAND·Product code FMI·November 22, 2024

    VITROS 5,1 FS CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JJE·December 17, 2007

    DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORPORATION·Product code KDI·October 24, 2014

    VITROS ECI IMMUNODIAGNOSTIC SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·August 11, 2011

    COULTER® AC*T DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·July 1, 2013

    PATIENT INTERFACE NIM4CPB1 NIM 4.0

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 28, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 7, 2016

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·January 24, 2014

    Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

    FDA Enforcement
    Class II ·Terminated·Becton Dickinson & Co.·August 28, 2019

    CANN CONNECTING SCR W/INTERNL THRD F/PERCUTAN INSERTN HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code FZX·August 28, 2017

    OLD 5ML CLR EXACTAMED EMEA (H9381105)

    FDA Adverse Event
    BAXTER HEALTHCARE CORPORATION·Product code KCP·November 21, 2013

    STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 11, 2016