BEUDAMED
    10 results · 20ms · 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 ×

    IQ FLEX M

    FDA Adverse Event
    Malfunction ·FIRST SOURCE INC.·Product code IZL·May 29, 2024

    iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System

    FDA 510(k)
    FDA Class 2 ·Radiology

    AltaTrack equipment, AltaTrack Guidewire, AltaTrack Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HUMAN IGG SUBCLASS LIQUID REAGENT KITS FOR USE ON THE HITACHI 911/7070 TURBIDIMETRIC ANALYSER

    FDA 510(k)
    FDA Class 2 ·Immunology

    IMPL TAPERED SCR-V HA 4.7 MM 4.5MM 10MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·August 5, 2019

    Widex

    FDA UDI
    Widex A/S·05706069809985·Widex EVOKE E-FS (Tan silk ) 220, Telecoil, RC ...

    IMPL TAPERED SCR-V HA 3.7 MM 3.5MM 10MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·December 14, 2024

    LCS COMP RP INSERT LG 17.5MM

    FDA Adverse Event
    Injury ·Product code NJL·November 3, 2014

    BIVONA UNCUFFED PEDIATRIC FLEX TEND PLUS TRACHEOSTOMY TUBE

    FDA Adverse Event
    Injury ·SMITHS MEDICAL ASD, INC.·Product code JOH·July 3, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 12, 2015