BEUDAMED
    10 results · 20ms · 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 ×

    BIOZ SYSTEM & BIOZ PORTABLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SIGMA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295250920·SIGMA CURVED PLUS INSERT TRIAL SIZE 1.5 8mm

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111048·INSTRUMENT CASE SMALL ALUMINUM

    SIMS DELTEC

    FDA Adverse Event
    Injury ·SIMS DELTEC·Product code FRN·October 20, 1997

    GREINER VACUETTE QUICKSHIELD COMPLETE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Neurostructures Cavetto® Cervical Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 21, 2013

    RENAISSANCE 26 P-WASS

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FPO·December 30, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 31, 2014

    PECTUS SYSTEM JANTON 12" TI PECTUS BAR 3.048CM (12") (L) TITANIUM

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 2, 2019