BEUDAMED
    14 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Microlife Upper Arm Automatic Digital Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CLARIS

    FDA UDI
    Oticon A/S·05707131318992·PZ100, BTE 13 WL 110 CNB CLARIS

    SPINAL ELEMENTS POSTERIOR CERVICAL/THORACIC SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEALTH MASK

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    TORNIER

    FDA Adverse Event
    Malfunction ·TORNIER INC.·Product code HWC·April 8, 2011

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 14, 2014

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FRN·May 24, 2013

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 21, 2011

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NIQ·June 29, 2018

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·February 21, 2018