BEUDAMED
    1,365 results · 32ms · Sources: EU EUDAMED, US FDA

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    MIRACLE - EAR MODEL PBP

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    PBP TOTAL HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OVALITH P-BP BIPOLAR CARDIAC PACEMAKER

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    BELMONT MODEL PBP INTRA-AORTIC BALLOON PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Seat Ergometer ergoselect 200 P BP

    FDA UDI
    ergoline GmbH·04059358000350·

    Seat Ergometer ergoselect 100 P BP

    FDA UDI
    ergoline GmbH·04059358000336·

    Recumbent Ergometer ergoselect 600 P BP

    FDA UDI
    ergoline GmbH·04059358001654·

    Seat Ergometer viasprint 150 P BP Viasys

    FDA UDI
    ergoline GmbH·04059358000268·

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIV·Product code FII·May 26, 2006

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB/MONITOR DIVISION·Product code MQS·February 23, 2006

    PRISMAFLEX M150

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MEYZIEU·Product code KDI·August 2, 2019

    Couch Ergometer ergoselect 1200 EL 230V P BP

    FDA UDI
    ergoline GmbH·04059358000374·

    PRISMAFLEX HF1400

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MEYZIEU·Product code KDI·April 18, 2018

    PRISMAFLEX M100

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MEYZIEU·Product code KDI·November 14, 2019

    PRISMAFLEX HF1400

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MEYZIEU·Product code KDI·March 26, 2018

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB·Product code KDI·February 23, 2006

    NI

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MEYZIEU·Product code KDI·August 6, 2019

    X SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·October 4, 2023

    PRISMAXPRISMAX SYSTEM

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDI·October 20, 2020

    PRISMAFLEX SYSTEM

    FDA Adverse Event
    Malfunction ·GAMBRO LUNDIA AB, MONITOR DIVISION·Product code KPF·October 27, 2006