BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    INTERSON MULTIPLANE RECTAL PROBE FOR ALOKA ULTRA.

    FDA 510(k)
    FDA Class 2 ·Radiology

    TEKMEDIC POWDERED SINGLE-USE LATEX PATIENT EXAMINATION GLOVES WITH PROTEIN & POWDER LABEL CLAIM CONTAINS 70MGM OR LESS O

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PLEGIOX CARDIOPLEGIA HEAT EXCHANGER WITH SOFTLINE COATING, MODEL BIO-CHX 30

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    1000 ML TPN BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·December 9, 2020

    VENTED MICRO VOL.INLET, N/S

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022

    250 ML TPN BAG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 21, 2021

    COBAS E 402 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 6, 2026

    REVEEL LAPAROSCOPIC RETRACTOR, RT

    FDA Adverse Event
    Malfunction ·MICROLINE SURGICAL·Product code GEI·September 10, 2025

    REVEEL LAPAROSCOPIC RETRACTOR, RT

    FDA Adverse Event
    Malfunction ·MICROLINE SURGICAL·Product code GEI·September 10, 2025

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 27, 2014

    ENDURANT II ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·January 7, 2013

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 29, 2010