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

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    TUFFCARE MEDICAL PRODUCTS WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756588270·OR TRAY

    NA

    FDA UDI
    STERILMED, INC.·10888551012799·DRILL BIT TWIST

    Reprocessed 2.0mm Drill Bit

    FDA UDI
    SURETEK MEDICAL·B390AR8944221·

    Arthrex

    FDA UDI
    Provision·B504OMAR8944220·

    Arthrex

    FDA UDI
    Provision·00810041063045·

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867052840·DRILL BIT, 2.0MM (AO)

    DRILL BIT, 2.0MM (AO)

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·June 20, 2023

    PHENYLETHYL ALCOHOL AGAR PLATE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    SERIES 25 SLIMLINE CRYO PROBES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867264717·2.0MM DRILL BIT, (AO), REUSABLE

    DRILL BIT, 2.0MM (AO)

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·March 4, 2024

    DRILL BIT, 2.0MM (AO)

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HTW·June 26, 2019

    SYMBIQ SCHANNEL 3.01

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 25, 2014

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 3, 2013

    RADIOTHERAPEUTICS RF 3000 RADIOFREQUENCY GENERATOR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code GEI·November 9, 2010

    Alaris System PC Unit Model 8000, a modular infusion pump and monitoring system

    FDA Enforcement
    Class I ·Terminated·CareFusion 303, Inc.·August 12, 2020