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

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    STRETCH VINYL EXAMINATION GLOVE, POWDER FREE (YELLOW/WHITE)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707065678·INTRAORAL ELASTICS 2,5 oz 3/8" orange

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482038727·Symmetry® Probe, Double-Ended, Stainless Steel,...

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450208779·

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345027244·Inserter, 11-16MM, Lumbar Straight

    HNM MEDICAL

    FDA UDI
    HNM STAINLESS, LLC.·00842962108758·PROBE, 8", DOUBLE ENDED, SS

    GEM PREMIER 3000- ADDITION OF GLUCOSE AND LACTATE AS NEW PARAMETERS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    C-IT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·May 14, 2019

    ILIAC SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MNH·October 16, 2019

    TENDRIL ST

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·May 2, 2013

    COLIBRI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·September 15, 2014

    4.0MM 90-S MAX SERFAS ENERGY SUCTION PROBE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·April 19, 2011

    POLARIS SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·January 8, 2020

    POWERLED

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·May 7, 2021

    NOVOSYN VIOLET 2/0 (3) 70CM HS 23 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL S.A.·Product code GAM·August 7, 2015

    POWERLED

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·November 21, 2022

    POWERLED

    FDA Adverse Event
    Malfunction ·MAQUET SAS·Product code FSY·November 17, 2022

    POLARIS TRANSLATION SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·November 27, 2019