BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    ProLift Pivot Expandable Spacer System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RELI NRFit Epidural Needles, Phoenix NRFit Epidural Needles, RELI NRFit Spinal Needles, Phoenix NRFit Spinal Needles

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Navio

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACU-LOC® 2 VDR PLT, NARROW, R

    FDA Adverse Event
    Injury ·ACUMED LLC·Product code HRS·November 23, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 23, 2024

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 11, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 12, 2011

    CORAIL2 STD SIZE 16

    FDA Adverse Event
    Injury ·Product code JDI·July 23, 2013

    ALINITY I RUBELLA IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LFX·November 26, 2025

    ALINITY I RUBELLA IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LFX·November 7, 2025

    ALINITY I RUBELLA IGG REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LFX·February 13, 2026