BEUDAMED
    9 results · 28ms · 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.
    Filters Regulation: Us FDA ×

    PEYMAN G. 12.12 YAG LASER LENS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556708054·GC Initial™ Zr-FS Enamel Occlusal EO-17, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228750871·GC Initial™ Zr-FS Enamel Occlusal EO-17, 20g

    Medtronic Reusable Instrument

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·20673978069146·DISTRACTOR 875-087 PINS STER 12MM

    VAN-TEC DOUBLE SHEATH GRASPING FORCEPS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LASERMATIC SURGILASER MODEL 5050

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

    TENDRIL STS

    FDA Adverse Event
    Death ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·June 16, 2014

    PFC*SIGMA C/R POR FEM LF SZ2

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·December 17, 2012

    NI

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code HSB·October 14, 2010