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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SOCT COPERNICUS, MODEL 15205

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SOLIDEA

    FDA UDI
    CALZIFICIO PINELLI SRL·08300496071839·STRIPE GAME IDRA, SIZE L, RUBINO, GRADUATED COM...

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 1, 2024

    DOXADENT DENTAL COMPOSITE, MODELS A, B, C, 12A, 12B, 12C, 6A, 6B, AND 6C

    FDA 510(k)
    FDA Class 2 ·Dental

    AART GLUTEAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MOTORIZED 3-WHEELED VEHICLE FOR OUTSIDE TRANSPORT

    FDA Adverse Event
    C.T.M. HOMECARE PRODUCT, INC·Product code INI·April 22, 2013

    GORE TEX VASCULAR GRAFT

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES, INC·Product code DSY·April 21, 2011

    TARGET DEVICE 300X160MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·July 8, 2008