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

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    BUN RATE REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ERA® ANGLE GAUGE KIT

    FDA UDI
    STERNGOLD DENTAL LLC·00841549116209·Used to choose the ERA® Implant Abutments which...

    APEX ARC HIP STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NAC PLUS NEEDLELESS ACCESS CONNECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 13, 2019

    BD SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·December 17, 2019

    SYRINGE S2 5ML 22GA 1-1/4IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·October 14, 2019

    HICKMAN 7 FR DUAL-LUMEN CV CATHETER, PEEL-APART INTRODUCER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (BARD)·Product code LJS·March 10, 2014

    CAPSUREFIX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 31, 2012

    PUMP MMT-522NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·August 9, 2010

    Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm; intended for use in long bone fractures, the fixation of osteopenic bone, the fixation of osteotomies, and for the fixation of non-unions and malunions.

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·September 30, 2015