BEUDAMED
    27 results · 31ms · Sources: EU EUDAMED, US FDA

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    ANATON

    FDA 510(k)
    FDA Class 2 ·Immunology

    Terumo® Advanced Perfusion System 1

    FDA UDI
    Terumo Cardiovascular Systems Corporation·00886799000557·The centrifugal control unit provides the local...

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209113613·KIT, TRAUMA & FIRST AID - CLASS A - HARD CASE w...

    PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIOPRO GLENOID COMPONENT W/ KEEL & W/ POSTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    Zimmer, Inc.·00889024156753·

    STAT SL 8.5 FR. 40 CC. IAB

    FDA Adverse Event
    Death ·DATASCOPE CORP.·Product code DSP·August 27, 1998

    ELECTRONIC GAS BLENDER

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·November 19, 2025

    STOCKERT S3 GAS BLENDER

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·December 22, 2014

    530G INSULIN PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·May 8, 2014

    HYDRATOME¿ RX 44

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNS·October 23, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 21, 2007

    S3 GAS BLENDER SYSTEM

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017

    S3 GAS BLENDER SYSTEM

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·October 16, 2017

    S3 ELECTRONIC GAS BLENDER

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DTX·December 19, 2024

    SORIN S3 GAS BLENDER

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND·Product code DTX·February 25, 2015

    ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.

    FDA Enforcement
    Class II ·Terminated·Olympus Corporation of the Americas·June 17, 2020

    Terumo Advanced Perfusion System 1 Control Unit; Catalog number 801046.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code DTQ·October 12, 2004

    Terumo Advanced Perfusion System 1 Integrated Centrifugal System Control Unit; Catalog No. 801046.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code DTQ·June 30, 2006

    Terumo Advanced Perfusion System 1 Integrated Centrifugal System Control Unit; Catalog number 801046.

    FDA Recall
    Terminated ·Terumo Cardiovascular Systems Corp·Product code DTQ·November 8, 2006