BEUDAMED
    21 results · 22ms · Sources: EU EUDAMED, US FDA

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    Ophthalmed Bending Laser Probes

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·14026704920645·

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704266498·FRAZIER TUBE 12 FRENCH

    CASTROVIEJO SUTURE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896015739·CASTROVIEJO SUTURE FORCEPS WITH TYING PLATFORM ...

    CASTROVIEJO SUTURE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896015654·CASTROVIEJO SUTURE FORCEPS WITH TYING PLATFORM ...

    Femtosecond Spatula

    FDA UDI
    Medetz Surgical Instruments LLC·G2231428300·Machat LASIK Retreatment Spatula DBL-Ended, Cyl...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A14283080·14mm H x 28mm W x 30mm L x 8 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A142830120·14mm H x 28mm W x 30mm L x 12 degrees ALIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587A142830150·14mm H x 28mm W x 30mm L x 15 degrees

    ZEOS

    FDA UDI
    SANTA BARBARA IMAGING SYSTEMS, INC.·00812231030943·C-MOUNT ARTHROSCOPE, 2.7MM 30DEG

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code KWP·March 31, 2016

    ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·August 8, 2016

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 23, 2014

    ZIMMER NATURAL NAIL CEPHALOMEDULLARY GUIDE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HSB·May 24, 2013

    EXCLAIM 8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 23, 2014

    SM104 MSERIES W5TH WHL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·June 20, 2011

    HANDPIECE MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·May 23, 2018