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

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    Filters Regulation: Us FDA ×

    INSULIN PEN NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172971185·

    TROPHON

    FDA 510(k)
    FDA Class 2 ·Radiology

    HERPES GROUP IGG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    STEM: AMISTEM H HA COATED STD STEM SIZE3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 17, 2019

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 29, 2025

    MITRACLIP

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code DRA·October 4, 2024

    PFC SIGMARP CV TB/IN S5 10.0

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

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 18, 2011

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·August 21, 2008

    MITRACLIP

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code DRA·November 15, 2024

    MITRACLIP

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL·Product code DRA·July 18, 2025

    UNKNOWN

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 20, 2025