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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    PERFECTA PDA TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SGARLATO FLEXIBLE HINGE TOE IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMFOR-DENT DENTURE LINER

    FDA 510(k)
    FDA Class 2 ·Dental

    PUMP MMT-515LNAP PRDGM INS V2.1 PL EN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·November 30, 2010

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·July 7, 2014

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·December 5, 2012

    BD BACTEC FX, INSTRUMENT TOP, PACKAGED

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·February 22, 2021

    Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-02, b) Medium, Item Number 314-02-03, c) Large, Item Number 314-02-04, Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024