BEUDAMED
    23 results · 34ms · Sources: EU EUDAMED, US FDA

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    Revolution Centrifugal Blood Pump

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REVOLUTION (ASSEMBLED INTO CUSTOMISED PERFUSION TUBING)

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·December 11, 2025

    REVOLUTION CENTRIFUGAL BLOOD PUMP COATED

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·November 11, 2024

    REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·December 2, 2022

    REVOLUTION PHISIO CENTRIFUGAL PUMP

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·June 23, 2021

    REVOLUTION PHISIO CENTRIFUGAL PUMP

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code KFM·May 20, 2021

    CENTRIFUGAL PUMP REVOLUTION 5

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·August 3, 2023

    CENTRIFUGAL PUMP REVOLUTION 5

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code KFM·August 3, 2023

    REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·September 14, 2022

    REVOLUTION CENTRIFUGAL BLOOD PUMP WITH PC COATING

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·March 17, 2023

    REVOLUTION CENTRIFUGAL BLOOD PUMP COATED

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code KFM·June 19, 2025

    REVOLUTION CENTRIFUGAL BLOOD PUMP

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA SRL·Product code KFM·March 19, 2022

    Pre-Finisher

    FDA UDI
    TP ORTHODONTICS INC·00192029042489·Asian 4 Bicuspid Extraction

    ZYSTON ARC INTERBODY SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPSMEDICAL VAPORIZED HYDROGEN PEROXIDE CHEMICAL INDICATORS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LOCKING SCREW, FULLY THREADED 5X55 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 30, 2010

    P850 CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER.·Product code FNL·October 3, 2008

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·June 26, 2013

    CLINAC

    FDA Adverse Event
    Malfunction ·VARIAN MEDICAL SYSTEMS, INC.·Product code IYE·July 27, 2011

    UNKNOWN LUMBAR IMPLANT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code MAX·April 11, 2022