BEUDAMED
    14 results · 19ms · Sources: EU EUDAMED, US FDA

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    MODIFIED PROFILE HIP ACETABULAR PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011891408000·discovery® delight Brackets single jaw + tubes...

    Nexxt Matrixx System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DISPOSABLE PRESSURE TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 7, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 6, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 27, 2018

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·April 16, 2018

    PRIDE MOBILITY PRODUCTS

    FDA Adverse Event
    Malfunction ·PRIDE MOBILITY PRODUCTS·Product code INO·June 24, 2014

    REFURBED COLLEAGUE CX VOLUMETRIC INFUSION PUMP SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 4, 2010

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·December 6, 2012

    BD VACUTAINER® CPT¿ NH: ~130 IU FICOLL¿: 2.0ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JCF·June 5, 2018

    GE HC OEC 9900 Elite and GE OEC 9800 Fluoroscopes Snubber Boards are a PCB with a 70 amp fuse to provide fused protection of internal system components from the high voltage system components, such as the X-ray tube or High Voltage Transformer. System model number A349855, Snubber Board number 00-880405-03 rev 5. This product is used for image intensified fluoroscopic x-rays for interventional radiologic procedures.

    FDA Enforcement
    Class II ·Terminated·GE OEC Medical Systems, Inc·August 29, 2012