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

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    ARCHITECT TACROLIMUS: MODEL 1L77

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 3, 2022

    ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 17, 2019

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345023871·BAYONETTED STRAIGHT RING CURETTE

    LYNX

    FDA UDI
    HNM TOTAL RECON LLC·00841742111360·LYNX ø4.0mm Cancellous Screw, Full Thread, Ti -...

    INFINION CX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 17, 2019

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 17, 2023

    MICROSCAN MICROSTEP PLUS PANEL NEW ANTIMICROBIAL - CEFUROXIME

    FDA 510(k)
    FDA Class 2 ·Microbiology

    AVANAR F/X 2.9F INTRAVASCULAR ULTRASOUND IMAGING CATHETER, MODEL 85700

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AXIUM 3D DETACHABLE COIL

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code HCG·April 22, 2013

    TPS UNIVERSAL DRIVER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HWE·April 15, 2011

    MICROSPEED UNI CONTROL UNIT W/COOL.UNIT

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code HBC·July 3, 2008

    DELTA CER INSERT 28ID X 50OD

    FDA Adverse Event
    Injury ·DEPUY IRELAND 9616671·Product code MRA·September 5, 2014

    Candela Smoothbeam Laser System Model Numbers: 9914-00-0820 9914-06-0820 9914-07-0820 9914-08-0820 9914-10-0820 Units are the same except for color

    FDA Recall
    Terminated ·Candela Laser Corporation·Product code GEX·November 25, 2003