BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    HEPARINIZED WOUND SUCTION TUBING

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Ortho Specialties

    FDA UDI
    Young Innovations, Inc.·00843471187128·Anatomical Molar Bands, Lower Right 2nd Molars,...

    POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Francisella tularensis Real-time PCR Assay

    FDA 510(k)
    FDA Class 2 ·Immunology

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 5, 2020

    POROUS NEXGEN TM PATELLA, 35MM DIA.

    FDA Adverse Event
    Injury ·ZIMMER TRABECULAR METAL TECHNOLOGY·Product code JWH·April 7, 2014

    12/14 ARTICUL 40MM M SPEC+8.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·September 26, 2012

    LAPAR COAGULATING SHEAR, 15MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·July 19, 2010

    Model Number U228, VISIONIST CRT-P EL MRI

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025