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 ×

    AUTO-LYTE COTININE EIA

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    Lacrimal Probe

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108680·MIYAKE LACRIMAL PROBE .45 AND .5MM

    IntelliCart System

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

    JET PORT PLUS HP CATHETER SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ENDOPATH ENDOSCOPIC LINEAR CUTTER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·May 20, 1997

    CORE IMPACTION DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·February 21, 2013

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·January 26, 2011