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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Aptima Herpes Simplex Viruses 1 & 2 Assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Oticon

    FDA UDI
    Oticon A/S·05707131305855·ACTO PRO, KIT 312 DIR R V BE RU

    RHEUMATOID FACTOR IMMUNOLOGICAL TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    MODIFICATION TO SYNGO INSPACE 4D

    FDA 510(k)
    FDA Class 2 ·Radiology

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·May 27, 2024

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·May 21, 2025

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 13, 2013

    ALTRUA

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 14, 2011

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·September 16, 2008

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·December 21, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EFB·November 26, 2025