BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DR180-R/OXY

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROXIMATE ILS CIRCULAR STAPLES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006

    HORIZON ORTHOPEDIC PIN PROTECTOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MISER CONTRAST MANAGEMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PROXIMATE ILS CIRCULAR STAPLERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.·Product code GAG·June 7, 2006

    ADVIA CENTAUR XP

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS·Product code MMI·February 28, 2013

    UNKNOWN DEPUY DURALOC LINER 50X28

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 31, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 6, 2014