BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    RA-1000 SYS-T4(THYROXINE)SERUM ANAL

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

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

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code FZP·June 15, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code FZP·June 8, 2006

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code FZP·June 7, 2006

    HARVARD APPARATUS INTERMITTENT INFUSION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TIA-IGA REAGENT & CALIBRATOR SETS

    FDA 510(k)
    FDA Class 2 ·Immunology

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 27, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·November 15, 2012

    EON 16-CHANNEL IPG

    FDA Adverse Event
    ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·September 1, 2010

    ELLIPSE DR, Tiered-therapy cardioverter/defibrillator, REF: CD2411-36Q, UDI: 05414734507615

    FDA Enforcement
    Class I ·Terminated·St Jude Medical Inc.·August 14, 2019