BEUDAMED
    87 results · 24ms · Sources: EU EUDAMED, US FDA

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    GRIPPER PLUS NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SEE H10

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KXA·November 1, 2011

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315809505·XL 1p36/1q25 del, 10x 100µl, Deletion Probe

    MODIFICATION TO FLEXVIEW CLINICAL MONITORING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TRIAGE TOX DRUG SCREEN CONTROLS, CATALOG #94001

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    Reicodent

    FDA UDI
    devemed GmbH·04061644029655·ECI | Esthetic composite instrument 1.0 / 1.0 m...

    Reicodent

    FDA UDI
    devemed GmbH·04061644029662·ECI | Esthetic composite instrument 1.5 / 1.5 m...

    Reicodent

    FDA UDI
    devemed GmbH·04061644029686·ECI | Esthetic composite instrument Occlusion f...

    Reicodent

    FDA UDI
    devemed GmbH·04061644029679·ECI | Esthetic composite instrument Flat plugge...

    TESTPACK PLUS HCG-COMBO

    FDA Adverse Event
    Other ·ABBOTT LABORATORIES, INC.·Product code JHJ·July 19, 1999

    AEMED STIMPAD ACU-TENS TRANSCUTANEOUS ELECTRICAL NERVE STIMULATOR, MODEL 021999

    FDA 510(k)
    FDA Class 2 ·Neurology

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·February 10, 2000

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·October 1, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·November 2, 1999

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·September 27, 1999

    2183157-1999-00323

    FDA Adverse Event
    Malfunction ·December 30, 1999

    9700 HEART RATE/RESPIRATION MONITOR

    FDA Adverse Event
    Malfunction ·NELLCOR PURITAN BENNETT·Product code FLS·January 4, 2000

    SOFTFORM FACIAL IMPLANT

    FDA Adverse Event
    Injury ·TISSUE TECHNOLOGIES, INC.·Product code FTL·September 27, 1999

    GLOBAL SHD HYL PEG GLENOID 44

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWS·July 23, 1999