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

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    The NOxBOXi Nitric Oxide Delivery System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AGXO

    FDA UDI
    Oticon A/S·05707131353603·G400 S, MINIRITE T 312 2.4G C063 AGXO

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113936·GIANNETTI "BIG SPURT" CANNULA 21GA

    24M - Tampa Electric Co.

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013497·24M Tampa Electric Co.

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383511278·"An absorbent paper points is an endodontic pap...

    3-PORT RADIAL VT

    FDA UDI
    The Wells Johnson Company·B458201339000·Cannula, 3-Port Radial VT, specify length, diam...

    MRI FASTSYSTEM RETRACTOR SYSTEM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE

    FDA 510(k)
    FDA Class 2 ·Microbiology

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·July 3, 2018

    NYLON SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAR·July 3, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·July 3, 2018

    ANIMAS VIBE SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·September 3, 2015

    ACRYSOF

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·January 13, 2014

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·January 7, 2014

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·August 26, 2013

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·January 7, 2014

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·August 2, 2013

    DIMENSION XPAND PLUS WITH HM

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·October 27, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 3, 2011

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 26, 2013