BEUDAMED
    17 results · 20ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO WOUN'DRES

    FDA 510(k)
    FDA Unclassified ·Unknown

    CAPENERGY - C100, C200, C300, C400, C50

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    WEDGELOC 180X STANDARD SUTURE ANCHOR WITH OPTI FIBER SUTURES,MODEL 1000-01 TAB VARYING DIAMETERS,

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MICROTAINER SST GOLD

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·June 7, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 1, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 16, 2018

    MICROTAINER SST GOLD

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON CARIBE LTD·Product code JKA·May 7, 2018

    BD MICROTAINER® EDTA LAVENDER TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·April 27, 2018

    BD MICROTAINER® EDTA LAVENDAR TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·May 3, 2018

    BD MICROTAINER® BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BD CARIBE LTD.·Product code JKA·December 3, 2017

    ACCESSORIES

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code DQX·March 20, 2025

    S-ROM*STM STD,30 NK,16X11X150

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code JDI·March 6, 2013

    PROTECTA XT CRT-D

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·February 15, 2011

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014

    PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACHEOSTOMY TUBE , Product Code/List Number/Item Code 60N025

    FDA Enforcement
    Class I ·Ongoing·Smiths Medical ASD Inc.·September 4, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·February 27, 2024

    INDEFLATOR

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR INC.·Product code MAV·March 21, 2024