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

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    FERTELL FEMALE FERTILITY TEST

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    EZflow

    FDA UDI
    MERCURY ENTERPRISES, INC.·10641043320020·

    MIS Bunion - 2.2 x 20mm Burr (47-0029-S)

    FDA UDI
    Eca Medical Instruments·00850078396020·

    Scott's Select Mirror Handle Cone Socket Round

    FDA UDI
    SCOTT'S DENTAL SUPPLY L.L.C.·D77810320021·Round cylindrical instrument handle to be used ...

    Ocata Anterior Cervical System

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

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0310020·Probe, 1.5 inch Ball, Steffee, Straight, Black

    CosmoLock Pedicle Screw System

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

    FPS

    FDA UDI
    Tyber Medical, LLC·00810040688911·5th Met. Avulsion Hook Plate Drill Guide, Right

    K032008

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007

    SUREFIT DISPERSIVE ELECTRODE

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

    VIKING OPTIMA GUIDING CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Kalitec Universal Instruments

    FDA UDI
    Kalitec Direct LLC·B07301K0380020·Handle, Ratcheting In Line Cannulated, Impact

    QUICK SET

    FDA Adverse Event
    Malfunction ·MAERSK MEDICAL A/S·Product code FPA·April 24, 2002

    SYNERGY

    FDA Adverse Event
    Malfunction ·INTERPACE CROSS INTERNATIONAL·Product code KWQ·March 20, 2003

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM 10.0CM

    FDA Adverse Event
    Injury ·BIOENTERICS CORPORATION·Product code LTI·May 15, 2002

    PROFILE MD V-186 SERIES TIERED THERAPY DEFIB.

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·March 15, 2002

    THERASPHERE

    FDA Adverse Event
    Death ·MDS NORDION·Product code KXK·May 12, 2003

    ETHICON

    FDA Adverse Event
    Injury ·ETHICON, JOHNSON & JOHNSON·Product code GAM·September 30, 2002

    THERASPHERE

    FDA Adverse Event
    Death ·MDS NORDION·Product code KXK·April 16, 2003

    13652067 12" 4-PANEL AB BINDER 46-62

    FDA Adverse Event
    Other ·DEROYAL INDUSTRIES, INC·Product code FSD·May 2, 2002