BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    GOTFRIED PERCUTANEOUS COMPRESSION PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DELFIA HLH SPEC KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    DISTAL TARGETING DEVICE R1.5

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·February 22, 2012

    PINN CAN BONE SCREW 6.5MMX15MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    SUMMIT POR TAPER SZ6 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    PINN CAN BONE SCREW 6.5MMX25MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018

    ISOFLEX S

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·February 28, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·February 10, 2011

    1.55 MM X 10 MM FLUTED TWIST DRL

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·December 18, 2013