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

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    VISCOUS FLUID INJECTOR SYSTEM MODULE (CX5700)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993039·anteriors; shade A2; mould BS

    Single Use Balloon Dilator V (with knife)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CONDOM (RUBBER) CONTRACEPTIVE

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

    FOLEY CATHETER, 2W SOFT VALVE STD 5/10CC CH14

    FDA Adverse Event
    Malfunction ·UNOMEDICAL SDN BHD·Product code KOD·March 1, 2013

    8800

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·February 8, 2011

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Injury ·MPRI·Product code NVN·August 8, 2014

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026