BEUDAMED
    14 results · 21ms · Sources: EU EUDAMED, US FDA

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    BUSSE PLASTIC TUBING CONNECTORS AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515244573·Suction/Irrigation Sheath, 4.0mm, tele 0 deg/25...

    COATED VICRYL* II

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MRP-7000: SUPPLEMENTAL R/F COILS

    FDA 510(k)
    FDA Class 2 ·Radiology

    D901 LILLIPUT OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·October 13, 2021

    ASR ACETABULAR IMPLANT 52

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 30, 2013

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·December 3, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 15, 2014

    CUSTOM PERFUSION PACK

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·October 30, 2012

    LILLIPUT 1 START

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 17, 2023

    LILLIPUT 1 OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALY·Product code DTZ·December 27, 2024

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 6, 2024

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·January 17, 2022

    LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·January 25, 2022