BEUDAMED
    22 results · 26ms · Sources: EU EUDAMED, US FDA

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    OSSIOfiber™ Hammertoe Fixation System/OSSIOfiber™ Hammertoe Fixation Implant

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017941·K-Wire, Double Ended, Trocar Point, Diameter Si...

    Pre-Finisher

    FDA UDI
    TP ORTHODONTICS INC·00192029042502·Asian 4 Bicuspid Extraction

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613017958·K-Wire, Double Ended, Trocar Point, Diameter 0....

    ALPHA DUO LAP INSUFFLATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ACL TIGHTROPE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN_MEDICAL_PRODUCT

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

    P850 CENTRA BED

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

    CLINAC

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

    REVOLUTION (ASSEMBLED INTO CUSTOMISED PERFUSION TUBING)

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

    I-STAT TROPONIN (CTNI) CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE·Product code MMI·June 5, 2019

    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

    AVAN REINF RING SS 48/58MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·December 29, 2025

    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