BEUDAMED
    9 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 ×

    BioCardia 8F Morph DNA Deflectable Guide Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AccuQuest

    FDA UDI
    Bernafon AG·05711584089064·AQ CO3 MNR, 2.4G NFM PB MAC/MSIL ACCUQ

    VACUETTE QUICKSHIELD WITH SNAPPY TUDE HOLDER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ATLAS INTERVERTEBRAL BODY CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PLUS SL

    FDA Adverse Event
    Injury ·SMITH & NEPHEW ORTHOPEDICS AG·Product code KWY·October 8, 2008

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD .·Product code MCM·June 27, 2013

    U BY KOTEX CLICK TAMPONS

    FDA Adverse Event
    Malfunction ·QINGDOA P&B CO. LTD·Product code HEB·May 27, 2011

    Aligned Medical Solutions, In House Ocular Pack, AMS12947A STERILEEO

    FDA Enforcement
    Class I ·Ongoing·Windstone Medical Packaging, Inc.·February 28, 2024

    METRX® SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HRX·May 2, 2023