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

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    Ventricular Catheter

    FDA 510(k)
    FDA Class 2 ·Neurology

    VITA TITANKERAMIK

    FDA UDI
    Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2009500·VITA TITANKERAMIK OPAQUE, B4, 50 g

    Pantheon System

    FDA UDI
    ADLER ORTHO SPA·08050880238149·Pantheon Shaft L95mm

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3

    IRIS SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896056060·IRIS SCISSORS WITH GOLD SCREW STRAIGHT TUNGSTEN...

    Avanos Cortrak 2 Enteral Access System (EAS)

    FDA Enforcement
    Class I ·Terminated·Avanos Medical, Inc.·May 25, 2022

    CORTRAK* 2 Enteral Access System (20-0950)

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

    EMBRYO TRANSFER CATHETER SET, MODEL 320200 AND 320201

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

    SPECTRAL'S 2 IN 1 (TNI-MYO)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MEDTRONIC ANEURX STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC CARDIOVASCULAR·Product code MIH·December 14, 2009

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 23, 2009

    SYNVISC ONE (HYLAN G-F 20) INJECTION 6/ML

    FDA Adverse Event
    Other ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·January 20, 2010

    ENDOSTAT II ELECTROSURGICAL UNIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·June 3, 2009

    COCR HEAD 28/+4 'L' 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code MEH·January 26, 2026

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    CORE MICRO DRILL

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code HBE·July 1, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    ANIMAS CORPORATION·Product code LZG·July 2, 2013

    ANCURE ENDOGRAFT (FORMERLY EVT ENDOGRAFT)

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·December 23, 2009

    ANCURE ENDOGRAFT (FORMERLY EVT ENDOGRAFT)

    FDA Adverse Event
    Injury ·GUIDANT ENDOVASCULAR SOLUTIONS·Product code MIH·December 23, 2009

    PROSTHESIS, RIB REPLACEMENT

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MDI·June 28, 2019