BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    L328 TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    MICROMAX L15

    FDA UDI
    Biomet Sports Medicine, LLC·00880304484948·

    POLAMEDCO NASOPAHARYNGEAL AIRWAY

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    ORTHOSORB(R) ABSORBABLE PIN

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COGNIS

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 9, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 1, 2014

    PRECISION XTRA/OPTIUM

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·December 5, 2007

    2.9MM MICROMAX ANCHOR FLEXIBLE LONG SHAFT WITH MAXBRAID SUTURE

    FDA Adverse Event
    Injury ·BIOMET SPORTS MEDICINE·Product code HWC·January 7, 2010

    Biomet 2.9 Micromax L-15 suture anchor, flexible long shaft, #2 blue/white maxbraid, PLLA/PGA L-15, sterile, Biomet Sports Medicine, Warsaw, IN; REF 905456. Intended for use in soft tissue reattachment procedures in the shoulder, wrist, elbow and knee.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code HWC·December 11, 2009