BEUDAMED
    8 results · 28ms · 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.

    D.O.R.C. HEXON ILLUMINATION SYSTEM

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

    Preview Digital Pregnancy Test

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NERVE MONITORING CABLE

    FDA 510(k)
    FDA Class 2 ·Neurology

    I-STAT CHEM8+ CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code JGS·November 21, 2017

    NON AC-POWERED PATIENT LIFT

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code FSA·February 21, 2013

    RX ACCULINK CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·Product code NIM·January 28, 2011

    RESOLUTION CLIP CLIPPING DEVICE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·August 1, 2014

    2.0 Mandible Locking Plate (MLP) Bender / Cutter (part number 329.143) Intended to be used for bending and/or cutting Mandible Locking Plates.

    FDA Enforcement
    Class II ·Terminated·Synthes, Inc.·February 4, 2015