BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    DERMATOPHYTIN O

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PULSE OXIMETER, MODELS CMS50E, CMS50F, CMS60C, CMS60D

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PACEMAKERS, VITATRONS (SERIES 3000)

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    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

    5CM HEAVY DUTY SHORT ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code HBC·May 5, 2014

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·October 15, 2012

    DUNLAP

    FDA Adverse Event
    Other ·KAZ, INC.·Product code IRT·August 3, 2010

    HF-RESECTION ELECTRODE

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

    TELESCOPE, 3 MM, 30°, WIDEANGLE, AUTOCLAVABLE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·April 25, 2023

    HF-RESECTION ELECTRODE

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

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025