BEUDAMED
    821 results · 23ms · 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 ×

    PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Preat

    FDA UDI
    Preat Corporation·00842092175590·Preci Post Yellow DDS Refill

    AFX MICROWAVE GENERATOR, FLEX ABLATION WAND, LYNX ABLATION WAND, MODEL SERIES 1000, P/N 102006, P/N 102007

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193108025·HA PEEK EVOS Straight, ,7mmx8mmx 30mm , FLAT 0...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694048866·PrimaLIF 7.5mm First Dilator

    Alliant Biotech

    FDA UDI
    MEDISURGE LLC·G6112201020070·Symmetric Total Knee Femoral Component Size 7 Left

    Symmetric TK Femoral Component

    FDA UDI
    SIGNAL MEDICAL CORPORATION·B0462201020070·7LT Symmetric TK Femoral Component

    SULZER VASCUTEK GELSOFT ERS VASCULAR PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    RHS HELMET

    FDA 510(k)
    FDA Class 2 ·Neurology

    ENDO CLIP 5MM CLIP APPLIER

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDO·May 11, 2007

    ACRYSOF TORIC

    FDA Adverse Event
    Other ·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·October 4, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON LABORATORIES INC./HUNTINGTON·Product code HQL·May 9, 2007

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON LABORATORIES,INC./HUNTINGTON·Product code HQL·May 9, 2007

    GORTEX GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE AND ASSOCIATES·Product code DSY·January 4, 2008

    SHUNT KIT, ULTRA SMALL, MEDIUM PRESSURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROSURGERY·Product code JXG·May 3, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·August 7, 2008

    ARTHROCARE TRISTAR 50

    FDA Adverse Event
    Malfunction ·ARTHROCARE·Product code HRX·June 17, 2005

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·April 9, 2008

    ENDO STITCH SHORT INSTRUMENT

    FDA Adverse Event
    Malfunction ·NORHT HAVEN - USS·Product code MFJ·December 10, 2007