BEUDAMED
    17 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    KRONUS OPTIQUANT THYROGLOBULIN KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    SKLARLITE RIGID STERILIZATION CONTAINER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BRUIS Software Suite

    FDA 510(k)
    FDA Class 2 ·Dental

    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 VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 4, 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

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 31, 2018

    BD VACUTAINER® CTAD BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·May 3, 2018

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F/7F

    FDA Adverse Event
    Injury ·ACCESSCLOSURE, INC.·Product code MGB·March 6, 2013

    CARELINK

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code KRG·August 8, 2014

    MARQUIS DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·February 15, 2011

    Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 11-114644S 11-114645 11-114646 11-114647 11-114648 11-114661 11-114662 11-114663 11-114664 11-114664S 11-114665 11-114666 11-114667 11-114668 11-114632 11-114633 Product Usage: Partial Shoulder Replacement.

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·December 4, 2019