BEUDAMED
    11 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    KetoSens Blood B-Ketone Monitoring System, KetoSens Multi Blood B-Ketone Monitoring System

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197070362·Davidson (scapula) Retractor 75x90m...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197070355·Davidson scapular retractor 75x50m...

    REVERA WOUND CARE, MODEL MDW0060

    FDA 510(k)
    FDA Unclassified ·Unknown

    PCECG-1200 SYSTEM WITH MODULAR ECG ANALYSIS SYSTEM (MEANS)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EMAX 2 PLUS MOTOR

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·June 14, 2013

    MINICAP

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

    G2 FILTER SYSTEM - FEMORAL

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·September 11, 2008

    MEDTRONIC HALL PROSTHETIC HEART VALVE

    FDA Adverse Event
    Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code LWQ·July 16, 2018

    MEDTRONIC HALL PROSTHETIC HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWQ·July 16, 2018

    OPEN PIVOT AP MITRAL HEART VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWQ·July 16, 2018