BEUDAMED
    9 results · 34ms · Sources: EU EUDAMED, US FDA

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    PNEUMATHERM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    FAC-5 - Class B 21 Kent - 5 Shelf Cabinet

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620893·FAC-5 - Class B 21 Kent - 5 Shelf Cabinet

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471123298·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 200mm

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471150607·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 230mm

    OSTIAL PRO STENT POSITIONING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EQUI-GUARD (ASPIRATOR FILTER)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNKNOWN TRIDENT ACETABULAR SYSTEM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS·Product code JDI·January 11, 2013

    GORE HYBRID VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DSY·December 7, 2010

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 9, 2014