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

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    RETIC-QUINOX

    FDA 510(k)
    FDA Class 2 ·Hematology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993496·anteriors; shade D4; mould CM

    NON-STERILE, POWDER-FREE, PINK LATEX EXAMINATION GLOVES WITH AND/OR WITHOUT STRAWBERRY SCENT AND WITH PROTEIN CONTENT

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CharmFil

    FDA 510(k)
    FDA Class 2 ·Dental

    9MM TI CANN TIBIAL NAIL-EX W/PROX BEND 300MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code JDS·September 21, 2017

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code IOR·March 7, 2013

    GIA 80-3.8 SINGLE USE RELOADABLE STAPLER

    FDA Adverse Event
    Injury ·USSC PUERTO RICO·Product code GDW·February 8, 2011

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NVZ·August 8, 2014

    SCRWDRVR F/4.5MM TI MULTILOC SCREWS/SLF-RETAIN/330MM

    FDA Adverse Event
    Malfunction ·SYNTHES HAGENDORF·Product code HXX·December 22, 2016

    Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017

    Presource Procedure Packs containing AAMI Level 3 surgical gowns, Multiple Catalog Numbers Produced Between September 1, 2018 and January 15, 2020

    FDA Enforcement
    Class II ·Terminated·Cardinal Health 200, LLC·February 26, 2020