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

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    Everest Spinal System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LACTOSORB® 2.0MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036123642·

    LACTOSORB® 2.0MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00888233012065·

    MaxFuse,VBR, 12 (D) x 14 (W) x 19 (H)

    FDA UDI
    Pioneer Surgical Technology, Inc.·00846468056018·12 (D) x 14 (W) x 19 (H)

    AIMSTICK URINE REAGENT STRIPS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MOVATION KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Injury ·RICE CREEK MFG·Product code LWP·June 7, 2013

    EASYTRAK 2

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·July 6, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 10, 2008

    AERO LL FIXATION ANCHOR, 50MM

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code OVD·March 25, 2019

    VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)

    FDA Enforcement
    Class II ·Terminated·Ortho-Clinical Diagnostics·November 28, 2018