BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    ANTI-HISTOPLASMA SERUM #CF10026X

    FDA 510(k)
    FDA Class 2 ·Microbiology

    TDS TITANIUM ABUTMENT FOR NOBEL BIOCARE BRANEMARK

    FDA 510(k)
    FDA Class 2 ·Dental

    AcQMap High Resolution Imaging and Mapping System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 15, 2012

    SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·May 22, 2015

    7700

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·August 6, 2010

    8F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL·Product code MGB·May 11, 2010

    REVITAN®, DISTAL PART, STRAIGHT, UNCEMENTED, 18/140

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HWC·July 24, 2024

    BIOLOX DELTA, CERAMIC FEMORAL HEAD, XL, 36/+7, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·August 7, 2018