BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    MASTERGRAFT RESORBABLE CERAMIC GRANULES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERASMART™

    FDA UDI
    Gc America Inc.·14548161320856·CERASMART™ 270 14L Universal A3 HT 5p Block

    CERASMART®

    FDA UDI
    Gc America Inc.·D0470125061·CERASMART 270 14L Unsvl A3 HT 5p

    n/a

    FDA UDI
    Ortho Development Corporation·00822409072576·Blunt Tip Broach Size 6

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707080572·ELASTIC WIRE FOR LIGAT./TRACTIONS 0,6

    READERS.COM

    FDA UDI
    FGX INTERNATIONAL INC.·00192304127863·

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0105060·Inserter Sleeve, All Size Implants

    READERS.COM

    FDA UDI
    FGX INTERNATIONAL INC.·00192304128068·

    neoWave LS

    FDA UDI
    XENIX MEDICAL LLC·00818345024243·Lumbar Inserter, Inline- Lateral

    READERS.COM

    FDA UDI
    FGX INTERNATIONAL INC.·00192304127900·

    READERS.COM

    FDA UDI
    FGX INTERNATIONAL INC.·00192304127887·

    OMNILINK .035 BILIARY STENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BREATHING FILTER FOR DISPOSABLE ANESTHESIA BREATHING CIRCUIT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PORTEX GENERAL ANESTHESIA CIRCUITS

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code CAI·May 18, 2022

    THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·August 14, 2013

    ZENITH FLEX AAA ENDOVASCULAR GRAFT BIFURCATED MAIN BODY

    FDA Adverse Event
    Malfunction ·COOK, INC.·Product code MIH·February 20, 2013

    S4S/SUR-FIT NATURA 2PC-2PC STOMAHESIVE (SH)

    FDA Adverse Event
    Injury ·CONVATEC INC.·Product code EXE·August 12, 2014

    LIBERTE' MONORAIL CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·March 12, 2008

    RETRACTA DETACHABLE EMBOLIZATION COIL

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·January 6, 2021

    Sheath Obturator, introducer, catheter. Obturator Accessory Kit Reorder number 406405, a 6 Fr, 15 cm length Obturator supplied as a 10-pack box with 10 Individually packaged Obturators. Sterile EO. Single use. St. Jude medical, DAIG Division, Inc., Minnetonka, MN 55345-2126 USA

    FDA Recall
    Terminated ·St. Jude Medical Daig Division·Product code DYB·September 20, 2005