BEUDAMED
    34 results · 23ms · Sources: EU EUDAMED, US FDA

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    B&J DVT Foot Garments, Models 820 Series

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EarQ

    FDA UDI
    Oticon A/S·05707131350886·G40 S, BTE PP 13 2.4G 105 C094 EARQ

    N/A

    FDA UDI
    HANS RUDOLPH, INC.·00874750002498·HEADGEAR SMALL V2MASK SPU

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111383458·DERF NH SERR 4 3/4"

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450258996·

    FLOWLINE BIOPORE EPTFE VASCULAR GRAFT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ETEST ESBL CT/CTL STRIP; ETEST ESBL TZ/TZL STRIP

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·June 20, 2018

    BLOOD GLUCOSE SYSTEM

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·October 5, 2015

    PROLIFT PELVIC FLOOR REPAIR UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·September 24, 2018

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·January 8, 2016

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·October 17, 2008

    SELECTION AFM

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code DXY·August 11, 2011

    PLV-102

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·June 26, 2013

    ARCHITECT ESTRADIOL

    FDA Adverse Event
    Malfunction ·A.I.D.D LONGFORD·Product code CHP·April 29, 2016

    HARMONIC ACE 5MM SHEAR

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·December 26, 2019

    MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 18, 2015

    MOSAIC

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 18, 2015

    HANCOCK II AORTIC CINCH 23

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 18, 2015

    MOSAIC

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 18, 2015