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

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    SYDNEY IVF CULTURE OIL

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

    OTS - Class B 21 Field Trauma - Hawkespack

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620022·OTS - Class B 21 Field Trauma - Hawkespack

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690126461·Adjustable Modular Tibia Tray Trial Size 2

    Ocata Anterior Cervical System

    FDA UDI
    Kalitec Direct LLC·B07308K0120020·Driver Shaft, Final Tighten

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0120020·T-Handle, T25, Screw Height Adjuster

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930702200200·Sterilization Case 2 Level

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197302203·Farrior Ear Specula, round inner ...

    SUREFIT DISPERSIVE ELECTRODE

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

    VIKING OPTIMA GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NCP PULSE GENERATOR

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·July 3, 2002

    PROFILE MD V-186 SERIES TIERED THERAPY DEFIB.

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·March 7, 2002

    LIFEPORT VASCULAR ACCESS SYSTEM

    FDA Adverse Event
    Malfunction ·HORIZON MEDICAL PRODUCTS, INC.·Product code LJT·February 26, 2002

    CONTOUR LABRAL NAIL

    FDA Adverse Event
    Other ·LINVATEC BIOMATERIALS, INC.·Product code MAI·April 5, 2005

    ANCURE ENDOGRAFT SYSTEM

    FDA Adverse Event
    Death ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·November 1, 2002

    SUBTALER M.B.A.

    FDA Adverse Event
    Injury ·KINETIKOS MEDICAL, INC.·Product code HRS·December 5, 2002

    PLASMACELL-C DISPOSABLE SET W/1000 ML BAG

    FDA Adverse Event
    Injury ·DOMINICAN REPUBLIC·Product code GKT·March 22, 2002

    SUBTALER M.B.A.

    FDA Adverse Event
    Injury ·KINETIKOS MEDICAL, INC.·Product code HRS·December 5, 2002

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL A/S·Product code FPA·March 6, 2002

    16 FR. ULTRAMER FOLEY TRAY

    FDA Adverse Event
    THE KENDALL COMPANY·Product code EZL·March 4, 2002

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL A/S·Product code FPA·March 6, 2002