BEUDAMED
    8 results · 18ms · 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 ×

    SAVE-T-BREATH AMBILICAL CORD CLAMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981152161·Ventura NM Trial, 11mm x 28mm x 13mm, Lordotic

    MODIFICATION TO SLIM GLIDING NAIL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM

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

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    PULSE GEN MODEL 102R

    FDA Adverse Event
    Injury ·CYBERONICS INC·Product code LYJ·January 29, 2013

    INTEGRATED APD SET W/CASSETTE3 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 21, 2010

    LOCKING SCREW ANCHORAGE Ø3.0MM / L16MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA SELZACH·Product code HRS·July 15, 2014