BEUDAMED
    1,214 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    HUMAPEN ERGO, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code KZE·February 25, 2003

    HUMAPEN ERGO, BURG-OPAQ/CLEAR CARTRIDGE HOLDER

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code KZE·April 7, 2006

    HUMAPEN ERGO, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code FMF·August 17, 2005

    HUMAPEN ERGO, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code NSC·April 16, 2004

    HUMAPEN ERGO, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code NSC·April 8, 2004

    HUMAPEN ERGRO, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code KZE·July 26, 2005

    HUMAPEN ERGO, TEAL, OPAQUE

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code KZE·June 3, 2005

    MEDFUSION MED PUMP

    FDA Adverse Event
    Malfunction ·MEDEXINC·Product code FRN·September 13, 2010

    ARROW PICC SET 2-LUMEN: 5 FR X 19-5/8" (50 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code LJS·September 20, 2024

    NOVUM IQ

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·October 7, 2025

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·April 4, 2016

    HUMAPEN EROG, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code FMF·August 18, 2003

    HUMAPEN ERGO 3 ML

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO.·Product code KZE·May 2, 2002

    HUMAPEN ERGO, TEAL/CLEAR

    FDA Adverse Event
    Malfunction ·ELI LILLY AND CO·Product code KZE·February 6, 2003

    AGILIA VP MC WIFI MX

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S·Product code FRN·April 27, 2026

    AGILIA VP MC WIFI MX

    FDA Adverse Event
    Malfunction ·FRESENIUS VIAL S.A.S·Product code FRN·April 27, 2026

    2-DAY INFUSION KIT W/4.16 CC/H

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code MEB·August 31, 2009

    FARADRIVE STEERABLE SHEATH CLEAR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRA·June 10, 2025

    MINIBORE BI-FUSE PRESSURE 2 IV CONNECTOR

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·April 23, 2021

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·July 17, 2020