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

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    Microlife Wrist Watch Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    McPHERSON NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896017542·McPHERSON NEEDLE HOLDER WITHOUT LOCK EXTRA DELI...

    McPHERSON NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896074392·McPHERSON NEEDLE HOLDER WITHOUT LOCK VERY DELIC...

    Flextrode

    FDA UDI
    COSMAN MEDICAL, LLC·08132500133826·Electrode 15cm, 13mm Tip, 20G

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694046848·PrimaLIF LLIF PEEK Implant, 13mm X 18mm X 30mm,...

    NA

    FDA UDI
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·00813250013382·Flextrode, 15cm,17G Introducer

    UVBIOTEK MODELS 3200B AND 4000B

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MIDWEST REPROCESSING CENTER REPROCESSED SCD EXPRESS SLEEVES/ FOOT CUFFS, MIDWEST REPROCESSING CENTER REPROCESSED ALP SLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·June 7, 2013

    CONFIRM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code MXC·January 13, 2014

    RESIDENT BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·June 7, 2011

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 19, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 20, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·September 9, 2025