BEUDAMED
    31 results · 20ms · Sources: EU EUDAMED, US FDA

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    MEDTRADE PRODUCTS ALGINATE ISLAND

    FDA 510(k)
    FDA Unclassified ·Unknown

    Sledgehammer

    FDA UDI
    Keystone Industries·H66810004871·SC 5 lb Pwd & 1 Qt Liq Kit, Clear

    Affiniti

    FDA UDI
    TORNIER, INC.·00846832023585·TUBEROSITY REAMER

    Leksell Stereotactic System

    FDA UDI
    Elekta Instrument AB·07340048304979·SLOTTED FRONT PIECE

    TEWA

    FDA UDI
    asia-med GmbH·04251282511050·TeWa CJ-Type 35100 Safe-T Sleeve: coated acupu...

    TEWA

    FDA UDI
    asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282503734·TeWa CJ-Type 35100 Safe-T Sleeve: coated acupu...

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167700004870·

    CURE™ ACP

    FDA UDI
    MEDITECH SPINE, LLC·B167S1700004870·

    MARHUKAR TRIPLE LUMEN CATHETER, MODEL 12 FR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BRAHMS DIAGNOSTICA LUMITEST ANTI-TPO

    FDA 510(k)
    FDA Class 2 ·Immunology

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO.·Product code FGE·November 21, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code FGE·November 5, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code FGE·February 20, 2009

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO.·Product code FGE·November 4, 2008

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Malfunction ·ANGIOMED GMBH & CO, MEDIZINTECHNIK·Product code FGE·February 13, 2009

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·March 12, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·February 1, 2011

    MODULAR ACETABULAR LINER

    FDA Adverse Event
    Injury ·BIOMET, INC.·Product code LPH·February 20, 2008

    BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE

    FDA Adverse Event
    Malfunction ·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026

    ANSPACH***REF 98-0035***Custom eMax 2 Plus Motor with microMax Disconnect Sleeve***Rx Only*** This device is intended to be used with Anspach Systems

    FDA Enforcement
    Class II ·Terminated·The Anspach Effort, Inc.·July 2, 2014