BEUDAMED
    8 results · 34ms · 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.

    KENDALL CURITY SUPRAPUBIC CATHETER TRAY, KIT, & REPLACEMENT SET

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

    URIC ACID REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code KNK·April 15, 2011

    CLEV-DENT COLHS ELECTROSURG, MOLEL TR-5

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

    Eclipse Treatment Planning System

    FDA 510(k)
    FDA Class 2 ·Radiology

    DENTAL FLOSS

    FDA Adverse Event
    Injury ·RANIR, LLC·Product code JES·June 30, 2014

    AJUST ADJUSTABLE SINGLE-INCISION SLING

    FDA Adverse Event
    Injury ·BARD SHANNON LIMITED·Product code FTL·February 15, 2013

    FIBER ONE

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·January 6, 2011

    Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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