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

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    CURBELL PATIENT MONITORING CABLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PULSION CONTINUOUS PULSE CONTOUR CARDIAC OUTPUT (PICCO) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HI-WAVE; POUR-PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 8, 2024

    PVA FOAM EMBOLIZATION PARTICLES

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KRD·March 26, 2018

    UNICEL® DXC 800 SYNCHRON® SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·April 29, 2013

    SECURE 2 MED/SURGBED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·April 13, 2011

    RSVR MMT-332A 10PK PRDGM 3CC 14L

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code FMF·July 18, 2008

    PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/CERAMIC/POLYMER, CEMENTED OR NON-POROUS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LZO·April 24, 2026