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

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    VIDAS C DIFFICILE GDH

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Port Access Kit

    FDA UDI
    Bard Access Systems, Inc.·00801741044182·PowerLoc MAX 20G X 1" with Y-Site PAK

    Port Access Needle

    FDA UDI
    Bard Access Systems, Inc.·00801741047350·PowerLoc Max 20G x 1 inch with y-site

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707066804·ELASTIC LIGATURES TRANSP 1,0mm

    MEGA PLUS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665580108·Rod(CoCr), Ø6.0 x 100mm

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021537·A-CIFT SoloFuse 4.2 Screw, Rigid, 16mm

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021513·A-CIFT SoloFuse 4.2 Screw, Rigid, 14mm

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021490·A-CIFT SoloFuse 4.2 Screw, Rigid, 12mm

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021520·A-CIFT SoloFuse 4.2 Screw, Rigid, 15mm

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361021506·A-CIFT SoloFuse 4.2 Screw, Rigid, 13mm

    VACUETTE PREMIUM SAFETY BLOOD COLLECTION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GLOVETEX POWDER FREE NITRILE EXAMINATION GLOVES, BLUE, NON-STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    INFANT DUAL-HEATED EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·January 12, 2011

    POWERLOC MAX POWER-INJECTIBLE INFUSION SET 20G X 1.0 IN

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code FPA·February 5, 2020

    ASKU

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 29, 2013

    ACCU-CHEK ULTRAFLEX INFUSION SET

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSTEMS·Product code FPA·August 19, 2008

    EQUOS BORDERED GAUZE 4X10

    FDA Adverse Event
    Malfunction ·BRADY TECHNOLOGY WUXI CO. LTD.·Product code KGX·February 9, 2012

    PROGENIX DBM PUTTY

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MBP·January 7, 2011

    SYBRONPRO XRT

    FDA Adverse Event
    Injury ·EBI INC.·Product code DZE·October 4, 2010