BEUDAMED
    8 results · 18ms · 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 ×

    PEGGED ACETABULAR COMPONENT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970501·anteriors; shade BL2; mould BOM

    CrossFT Knotless Biocomposite Suture Anchor with Disposable Driver

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RUIKE 3421 POWERED WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013

    JETSTREAM G3

    FDA Adverse Event
    Injury ·PATHWAY MEDICAL TECHNOLOGIES, INC.·Product code MCW·January 20, 2011

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019