BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    DropSafeTM SicuraTM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CIQ CONTROLLER, CIQ WANDS

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

    SYDNEY IVF HYALURONIDASE

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

    PERMANENT CAUTERY SPATULA INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·November 4, 2014

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·August 17, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 12, 2013

    MAKO Integrated Cutting System (MICS) HANDPIECE, Catalog Number 209063

    FDA Enforcement
    Class II ·Ongoing·Howmedica Osteonics Corp.·October 16, 2024

    SpF PLUS-Mini (60 ¿A/W) Implantable Spinal Fusion Stimulator SpF PLUS-Mini Implantable Fusion Stimulators are indicated as a spinal fusion adjunct to increase the probability of fusion success in 1 or 2 levels

    FDA Enforcement
    Class I ·Terminated·Zimmer Biomet, Inc.·November 7, 2018