BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    BLOOD COLLECTION TUBE HOLDER VANISHPOINT TUBE HOLDER/SMALL TUBE ADAPTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    AMADEUS ADAPTIVE COMPRESSION THERAPY

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HEMO-RO

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 6, 2013

    SYNCHRON LX® I 725 CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·January 27, 2011

    REVISION BASEPLATE -

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JWH·July 31, 2014

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·July 25, 2025

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024