BEUDAMED
    27 results · 25ms · Sources: EU EUDAMED, US FDA

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    SYMBIQ INFUSION AND ADMINSTRATION SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00850038691011·

    BD MAX¿ ENTERIC BACTERIAL PANEL

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code OOI·October 6, 2022

    Matira

    FDA UDI
    Kalitec Direct LLC·B07307K1100010·Tray Insert 1, Matira, Arcamed

    IPL THERAPY SYSTEM

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

    FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IMN) MODEL B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TPS

    FDA UDI
    STRYKER CORPORATION·04546540991690·Connector Cleaner

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090101500·BONE SCREW, 6.5MM DIAMETER, 15MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090104000·BONE SCREW, 6.5MM DIAMETER, 40MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090103500·BONE SCREW, 6.5MM DIAMETER, 35MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090102500·BONE SCREW, 6.5MM DIAMETER, 25MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090105000·BONE SCREW, 6.5MM DIAMETER, 50MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090102000·BONE SCREW, 6.5MM DIAMETER, 20MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090103000·BONE SCREW, 6.5MM DIAMETER, 30MM LENGTH

    Iconacy i-Hip

    FDA UDI
    Iconacy Orthopedic Implants LLC·M914011090104500·BONE SCREW, 6.5MM DIAMETER, 45MM LENGTH

    FEMORAL MODULAR HEAD

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·January 30, 2024

    ARCHITECT C4000 ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JGS·December 15, 2011

    ADULT DUAL-HEATED WITH EVAQUA BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZE·November 7, 2011

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·November 21, 2022

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 8, 2013