BEUDAMED
    14 results · 18ms · Sources: EU EUDAMED, US FDA

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    OPHTHALMIC VISCOINJECTOR DRIVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LODI Unified School Distric - 16 Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588233260·LODI Unified School Distric - 16 Poly White

    Axiom PSR System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SHERPA PAK CARDIAC TRANSPORT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TIBIAL NAIL, STANDARD 10X390 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·March 17, 2010

    CONVERTBL I.V.DUAL CHANNEL HSP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·December 20, 2011

    CONVERTBL I.V..DUAL C

    FDA Adverse Event
    Malfunction ·HOSPIRA LTD.·Product code FPA·August 13, 2009

    PRIMARY PLUMSET PP YSITE 272CM NDEHP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 19, 2012

    CONVERTBL I.V. DUAL C

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 15, 2009

    CONVERTBL I.V. DUAL CHANNEL HSP

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 7, 2011

    UNK

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·October 15, 2009

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Injury ·HEARTWARE, INC·Product code DSQ·July 17, 2015

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC·Product code NBW·September 1, 2016