BEUDAMED
    9 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.

    ANNULAR ARRAY SCANHEAD

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704294231·

    ZIMMER M/L TAPER HIP PROSTHESIS WITH KINECTIV TECHNOLOGY SYSTEM, MODEL(S) 7848 SERIES( MODULAR NECKS), 7713 SERIES

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    DIR. QUANT. COLOR. DETERM. SERUM CREAT.

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 13, 2014

    SYNCHRON® LX®I 725 CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·October 16, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·December 13, 2012

    UNK_PHACO METAL TIP WRENCH

    FDA Adverse Event
    Malfunction ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code HQC·March 11, 2026

    UNK_PHACO HANDPIECE

    FDA Adverse Event
    Malfunction ·AMO MANUFACTURING USA, LLC·Product code HQC·March 11, 2026