BEUDAMED
    7 results · 24ms · 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 ×

    DIGITAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRIATHLON KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    N-Force Fixation System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3DKNEE

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code JWH·June 5, 2014

    TWINFIX ULTRA - TI ANCHOR

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MANSFIELD MANUFACTURING SITE·Product code MBI·November 29, 2012

    INTERSTIM II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·September 30, 2010

    Philips Zenition 50, Model Number: 718096

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024