BEUDAMED
    10 results · 27ms · 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.

    MB/BACT MYCROBACTERIA DETECTION SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DIRECT BILIRUBIN REAGENT, 7776/7777/7576/7476/7176

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PORTALASE 200 CARBON DIOXIDE SURG LASER NEUROLOGIC

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

    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

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MPRI·Product code LWS·February 11, 2013

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    UNKNOWN·Product code IKX·July 24, 2014

    UNKNOWN DEPUY HEAD BALL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·January 5, 2011

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022