BEUDAMED
    38 results · 22ms · Sources: EU EUDAMED, US FDA

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    Li-Battery powered OTC TENS/EMS Combination Stimulator

    FDA 510(k)
    FDA Class 2 ·Neurology

    Skin Temp Probe, ¼” 3M

    FDA UDI
    DRAEGER MEDICAL SYSTEMS, INC.·04049098008730·

    AGXO

    FDA UDI
    Oticon A/S·05707131353566·G400 S, MINIRITE T 312 2.4G C091 AGXO

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116020508·Dornier Medilas H 400 Micron Single Use Laser F...

    Accufit

    FDA UDI
    Ortho Organizers, Inc.·00190707183820·Accufit Molar Bands Lower Right First Molar 33 1/2

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383511230·"An absorbent paper points is an endodontic pap...

    MONARCH SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACUMATCH L-SERIES CEMENTED FEMORAL STEM, MODEL L-SERIES CEMENTED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EPICEL

    FDA Adverse Event
    Death ·GENZYME BIOSURGERY (CAMBRIDGE)·Product code OCE·December 12, 2013

    EPICEL

    FDA Adverse Event
    Death ·GENZYME BIOSURGERY (CAMBRIDGE)·Product code OCE·November 5, 2013

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 15, 2014

    PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 15, 2014

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 15, 2014

    HS III PROXIMAL SEAL SYSTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·May 20, 2014

    HS III PROXIMAL SEAL SYTEM 3.8MM

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 15, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 9, 2013

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 27, 2014

    HEARTSTREAM FR2

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

    RESTORE PRIME ADVANCED

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

    HS III PROXIMAL SEAL

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·May 20, 2014