BEUDAMED
    16 results · 27ms · Sources: EU EUDAMED, US FDA

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    TRACTION ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    Sphero Attachment

    FDA UDI
    Preat Corporation·00842092115534·Sphero Flex Abutment Genesis Tapered 3.8mm x 3mm

    CODMAN® HAKIM®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780534907·CODMAN® HAKIM® Precision Fixed Pressure Valve, ...

    Obtura Spartan

    FDA UDI
    Young Innovations, Inc.·00843471152287·Multi Tool Obtura III @ Max

    BIPOLAR FORCEPS

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

    VASCULAR POSITIONING SYSTEM (VPS) G4 CONSOLE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRECISION VALVE INLINE, SIPHONGUARD

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·March 31, 2016

    FREESTYLE FREEDOM LITE

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 22, 2009

    CRIT-LINE BLOOD CHAMBER

    FDA Adverse Event
    Malfunction ·CONCORD MANUFACTURING·Product code KOC·February 20, 2014

    MICROPLEX (MCS) 10-SYSTEM COIL

    FDA Adverse Event
    Injury ·MICROVENTION, INC.·Product code HCG·October 29, 2012

    VERIFLEX (LIBERTE) CORONARY STENT DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·September 2, 2010

    PRECISION VALVE INLINE, SIPHONGUARD

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·April 14, 2017

    PRECISION VALVE INLINE, SIPHONGUARD

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC.·Product code JXG·August 11, 2014

    PRECISION VALVE INLINE, SIPHONGUARD

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·April 6, 2016

    PRECISION VALVE INLINT, SIPHONGUARD

    FDA Adverse Event
    Malfunction ·CODMAN & SHURTLEFF, INC. / MEDOS S.A.·Product code JXG·June 2, 2015

    Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty

    FDA Enforcement
    Class II ·Ongoing·Exactech, Inc.·April 10, 2024