BEUDAMED
    121 results · 21ms · Sources: EU EUDAMED, US FDA

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    VeriSight Intracardiac Echocardiography (ICE) Catheter, VeriSight Pro ICE Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694060837·2.0/2.4mm Angled Locking Plating Module, ICON

    Conventional Lead Apron .5mm Small 22 X 33

    FDA UDI
    Flow X Ray Corporation·00843696123017·Conventional Lead Apron .5mm Small, Purple

    Zavation

    FDA UDI
    Zavation LLC·00842166131927·Ti3Z CIF 12mmx14mmx12mm -8 deg

    FOMON-DORSAL SCISSORS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896055797·FOMON-DORSAL SCISSORS POWER CUT BLACK

    ULTICARE DISPOSABLE PEN NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NEURO SCAN MEDICAL SYSTEMS, MODELS 302L MEDICOR (LABORATORY) AND 302P ADVANTAGE 3000 (PORTABLE)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·January 8, 2009

    ACRYSOF

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·December 19, 2008

    Widex

    FDA UDI
    Widex A/S·05706069724516·Widex UNIQUE U-CIC L (Clay brown S-440 ) Left, ...

    Widex

    FDA UDI
    Widex A/S·05706069724875·Widex D-CIC (Clay brown S-440 ) Left, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069725230·Widex EVOKE E-IP (Clay brown S-440 ) Right

    Widex

    FDA UDI
    Widex A/S·05706069725834·Widex EVOKE E-CIC (Clay brown S-440 ) Left, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069726350·Widex Mind440 M4-X ITE (Clay brown S-440 ) Tele...

    TIMAX

    FDA Adverse Event
    Malfunction ·NSK TOCHIGI-KEN·Product code EGS·June 2, 2009

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·December 16, 2019

    TRUERESULT

    FDA Adverse Event
    Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·August 13, 2015

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·February 22, 2007

    MEDIUM COMPLEXITY MEDIA TEST KIT

    FDA Adverse Event
    Malfunction ·IVQA·Product code JSE·February 23, 2021

    TIMAX

    FDA Adverse Event
    Injury ·NSK·Product code EGS·May 27, 2010