BEUDAMED
    29 results · 30ms · Sources: EU EUDAMED, US FDA

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    HBP7 Settable Hemostatic Bone Putty

    FDA 510(k)
    FDA Unclassified ·Unknown

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113394·MICS TRAP KNIFE 1.8/2.2 (BX/5)

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113301·STAB KNIFE 45 DEGREE (BX/5)

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113387·ALIO MICS TRAP KNIFE (BX/5)

    SJM TAILOR ANNULOPLASTY BAND, MODEL TAB-(SIZE) (TAILOR BAND)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDOVATIONS ESOPHAGEAL DILATOR

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

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDT·January 10, 2024

    GORE® TAG® CONFORMABLE THORACIC STENT GRAFT WITH ACTIVE CONTROL SYSTEM

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·January 28, 2024

    ICYHOT HEAT THERAPY PATCHES

    FDA Adverse Event
    Injury ·CHATTEM, INC.·Product code IMD·October 14, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·August 2, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2013

    UNKNOWN ANGIO-SEAL VASCULAR CLOSURE DEVICE,OUS

    FDA Adverse Event
    Injury ·TERUMO MEDICAL CORPORATION·Product code MGB·July 18, 2023

    EVOLUT R TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·April 9, 2024

    VALIANT NAVION

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code MIH·May 3, 2024

    ESTROGEN RECEPTOR CLONE 6F11 READY-TO-USE PRIMARY ANTIBODY FOR BOND¿

    FDA Adverse Event
    Injury ·LEICA BIOSYSTEMS NEWCASTLE LTD·Product code MYA·January 10, 2024

    ESTROGEN RECEPTOR CLONE 6F11 READY-TO-USE PRIMARY ANTIBODY FOR BOND¿

    FDA Adverse Event
    Injury ·LEICA BIOSYSTEMS NEWCASTLE LTD·Product code MYA·January 10, 2024

    UNKNOWN TICRON

    FDA Adverse Event
    Injury ·DAVIS & GECK CARIBE LTD·Product code GAT·September 6, 2023

    GORE® EXCLUDER® ILIAC BRANCH ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·February 7, 2024

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·February 20, 2024

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·January 26, 2024