BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    CULTURE TUBE, (VACUTAINER)

    FDA 510(k)
    FDA Class 1 ·Microbiology

    Daytona

    FDA UDI
    Seaspine Orthopedics Corporation·10889981131678·Closed Lateral Connector, 4.5 x 5.5 x 45mm

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110669·COAXIAL IRR-ASP- TIP 90 DEG- W/ SILICONE

    Persona® Knee System

    FDA UDI
    Zimmer, Inc.·00889024658608·

    Persona® Knee System

    FDA UDI
    Zimmer, Inc.·00889024658592·

    ONCOBIONIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    I.T.S. PRS Phoenix II

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DEPUY ASR FEM IMPLANT SZ 49

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·September 26, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·December 18, 2013

    APEX MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·July 16, 2010

    Model Number U228, VISIONIST CRT-P EL MRI

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