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

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    TALYMED

    FDA 510(k)
    FDA Unclassified ·Unknown

    Preat

    FDA UDI
    Preat Corporation·00842092175576·Preci Post DDS refill. Kit contains:. 50 Yellow...

    Mini Master Series

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746108396·DB BKT MINI MS UL CEN 018 T+24 A+3 R=0

    FRAXEL

    FDA UDI
    SOLTA MEDICAL·00816995027454·ASSY, FOOTSWITCH, FRAXEL

    Integrity-SI Fusion System

    FDA UDI
    Lincotek Medical LLC·B57112524102002D0·Short 3.2mm Guide Pin

    Tubing Cartridge Set, M3000, Pack 2

    FDA UDI
    Medical Technical Products, Inc.·00850039020285·

    3.2mm K-wire - Short

    FDA UDI
    Osteocentric Technologies, Inc.·00810097800274·3.2mm K-wire - Short

    ROD, FIXATION, INTRAMEDULLARY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·August 9, 2016

    SUREFIT DISPERSIVE ELECTRODE

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

    VIKING OPTIMA GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD INJECTOR LUER LOCK N35

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·October 5, 2021

    25 G X 1 IN. ECLIPSE NEEDLE SMARTSLIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·September 1, 2021

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 22, 2013

    HUDSON ET TUBE, PREFORMED UNCUFFED NASAL, 5.0

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code BTR·September 15, 2014

    THERMACARE MENSTRUAL (THERMACARE HEATWRAP) WRAP

    FDA Adverse Event
    Malfunction ·PFIZER CONSUMER HEALTH CARE·Product code IMD·May 19, 2011

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 13, 2014

    ROD, FIXATION, INTRAMEDULLARY

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HSB·July 25, 2016

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·December 16, 2019

    Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

    FDA Recall
    Open, Classified ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025