BEUDAMED
    15 results · 27ms · Sources: EU EUDAMED, US FDA

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    Automatic Arm Bluetooth Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ers2 1CH ECG Transmitter Set (Adapter)

    FDA UDI
    ergoline GmbH·04059358001777·

    Drill Stopper for Long L16 1846

    FDA UDI
    ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157522·

    CONTIPLEX C CONTINUOUS PERIPHERAL NERVE BLOCK NEEDLE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    COMBI SCAN100

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BD 3ML SYRINGE LUER-LOK TIP WITH BD PRECISIONGLIDE NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·August 27, 2021

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929037041·Corpectomy, 16Dx18Wx46H 6°

    Matrixx System

    FDA UDI
    NEXXT SPINE, LLC·00889929066072·Corpectomy, 16Dx18Wx46H 0°

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    UNKNOWN PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·October 10, 2014

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

    JOURNEY GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·July 14, 2011

    STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code HRS·January 10, 2019