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

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    MACY CATHETER

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

    Oticon

    FDA UDI
    Oticon A/S·05707131264930·RIA, KIT 312 WL DIR 90 R V BE

    K133801

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 31, 2024

    MEDRAD STELLANT CT INJECTOR SYSTEM WITH IMAGING SYSTEM INTERFACE MODULE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEARTSINE SAMARITAN PAD 350P

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 26, 2021

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 27, 2020

    LCS TEX ROT PLAT TIB PLAT STD+

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code NJL·May 29, 2013

    RX VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code LIT·June 20, 2011

    ASR UNI FEMORAL IMPL SIZE 51

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·October 2, 2014