BEUDAMED
    13 results · 22ms · 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 ×

    Hypervisor IX Monitoring System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Leg Bag

    FDA UDI
    C. R. Bard, Inc.·00801741050848·Dispoz-A-Bag, Leg Bag with Flip-Flo Drainage Va...

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100110·FEASTER SPECULUM SOLID WIDE

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171027959·PESSARY, CUP #1, W/SUPPORT, 55/23mm

    BD SYRINGE LUER-LOK¿ TIP

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 22, 2017

    LUCENT OR LUCENT MAGNUM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADVIA IMS DIRECT HDL CHOLESTEROL ASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SYRINGE 30ML LL TIP CONV PAK

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMF·October 17, 2023

    RADIFOCUS OPTITORQUE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·June 13, 2022

    FIBERED IDC OCCLUSION SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code KRD·June 6, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    LONG NAIL KIT R2.0, STST, LEFT 11X400MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 23, 2011

    OPTITORQUE ANGIOGRAPHIC CATHETER

    FDA Adverse Event
    Malfunction ·Product code DQO·January 20, 2021