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

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    TRUFREEZE SYSTEM, TRUFREEZE SPRAY KIT

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

    8920 MASK

    FDA UDI
    HANS RUDOLPH, INC.·00817136020525·8920 ADULT LG MASK/2700 2W

    CapSure® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642103977·LP Cross Connector Medium

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1430210·Rod Template, 500mm

    ELEMENT PLUS BLOOD GLUCOSE MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LIGHTLANCE LASER SKIN PERFORATOR

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

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 12, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 12, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 11, 2024

    CARDINALHEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 13, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 12, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 13, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 12, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·3005670221-2024-00010 CARDINAL HEALTH JIA·Product code FMF·April 12, 2024

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 11, 2024

    CARDINALHEALTH

    FDA Adverse Event
    Malfunction ·JIANGSU CAINA MEDICAL CO., LTD.·Product code FMF·April 11, 2024

    LOCKING HOLDING SLEEVE- STANDARD FOR MATRIX

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·May 15, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 24, 2014

    AFFINITY BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 25, 2011

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015