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

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    Bioliner

    FDA 510(k)
    FDA Class 2 ·Dental

    MINISPACER DUAL-SPRAY MDI ADAPTER WITH 22MM (OR 15MM) OD / 22MM OD/ID CONNECTIONS / 15MM ID CONNECTIONS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OSTEOSPRING FOOTJACK SUBTALAR IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    T7 DRIVER CANN AO

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LXH·July 14, 2016

    ACTIVA

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    VASOVIEW HEMOPRO ENDOSCOPIC VESSEL HARVESTING SYSTEM

    FDA Adverse Event
    Malfunction ·GUIDANT CORPORATION, CARDIAC SURGERY·Product code GEI·September 25, 2008

    Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve D-F, Model A-TCSE-DF, Sterile.

    FDA Enforcement
    Class II ·Ongoing·Abbott·April 27, 2022