BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    PMT Facet Fixation System (PMT FFS)

    FDA 510(k)
    FDA Unclassified ·Unknown

    Tizian Blank 5.0

    FDA UDI
    Pritidenta GmbH·04251366906345·

    H/S CATHETER SET (5F), MODEL 61-5005; H/S CATHETER SET (7F), MODEL 61-5007

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    SMARTBUILDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·April 19, 2023

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·November 3, 2014

    CUSTOM DEFIND PRODUCT

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·August 23, 2011

    RETEX SUPPORT PP HALO NEEDLE KIT X1

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code OTN·July 3, 2013

    PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code LPH·October 17, 2025