BEUDAMED
    37 results · 30ms · Sources: EU EUDAMED, US FDA

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    Fujifilm Ultrasonic Processor

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517295835·CoRoent® XL-H, 8x22x50mm 20°

    VITA TITANKERAMIK

    FDA UDI
    Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2008500·VITA TITANKERAMIK OPAQUE, B3, 50 g

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046149·LATERAL IMPLANT, WIDE, STANDARD, 8mm X 23mm X 50mm

    Zavation

    FDA UDI
    Zavation LLC·00842166123342·Lateral Offset

    GPF-29 GENERAL PURPOSE COIL SET

    FDA 510(k)
    FDA Class 2 ·Radiology

    COWELL IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Widex

    FDA UDI
    Widex A/S·05706069725247·Widex EVOKE E-IP (Dark brown S-110 ) Right

    Widex

    FDA UDI
    Widex A/S·05706069725841·Widex EVOKE E-CIC (Dark brown S-110 ) Left, RC ...

    Widex

    FDA UDI
    Widex A/S·05706069724882·Widex D-CIC (Dark brown S-110 ) Left, RC coil

    Widex

    FDA UDI
    Widex A/S·05706069724523·Widex UNIQUE U-CIC L (Dark brown S-110 ) Left, ...

    UNKNOWN CERECYTE MICROCOIL

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2017

    UNKNOWN CERECYTE MICROCOIL

    FDA Adverse Event
    Death ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2017

    UNKNOWN CERECYTE MICROCOIL

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2017

    UNKNOWN CERECYTE MICROCOIL

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code HCG·June 9, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    INFUSOR LV10 SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code MEB·October 20, 2008

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 8, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

    ONYX

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code MFE·April 21, 2015