BEUDAMED
    9,598 results · 46ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    ELECTROPHORESIS WORK CENTER (EWC)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SPiN EWC – Biopsy Guide Kit

    FDA UDI
    VERAN MEDICAL TECHNOLOGIES INC.·00815686021108·

    EWC: ECG CABLE AND LEADWIRE SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EWC: ECG II CABLE LEADWIRE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BRONCHUS SYSTEM EXTENDED WORKING CHANNEL

    FDA Adverse Event
    Malfunction ·SUPERDIMENSION, LTD.·Product code KPR·October 19, 2006

    EDGE CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·SUPERDIMENSION INC.·Product code JAK·October 1, 2015

    3004659744-2006-00005

    FDA Adverse Event
    Malfunction ·Product code KPR·January 30, 2007

    COBAS INTEGRA 400 PLUS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 26, 2013

    BRONCHUS SYSTEM EXTENDED WORKING CHANNEL

    FDA Adverse Event
    Malfunction ·SUPERDIMENSION, LTD.·Product code KPR·October 19, 2006

    SPiN EWC – 90 degrees w/Locking Device, Olympus

    FDA UDI
    VERAN MEDICAL TECHNOLOGIES INC.·00815686021092·

    ILLUMISITE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·August 1, 2024

    ILLUMISITE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·October 2, 2024

    I-LOGIC INREACH SYSTEM

    FDA Adverse Event
    Injury ·SUPERDIMENSION INC.·Product code JAK·November 3, 2015

    ILLUMISITE

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code JAK·February 24, 2021

    ILLUMISITE ENDOBRONCHIAL PROCEDURE KIT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code JAK·October 4, 2023

    EDGE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·September 26, 2025

    ILLUMISITE

    FDA Adverse Event
    Injury ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·August 4, 2021

    EDGE CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·September 13, 2018

    ILLUMISITE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·October 2, 2024

    EDGE

    FDA Adverse Event
    Malfunction ·COVIDIEN LP - SUPERDIMENSION INC·Product code JAK·November 26, 2019