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

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    K-ASSAY IGM

    FDA 510(k)
    FDA Class 2 ·Immunology

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993323·anteriors; shade C1; mould UIL

    RESECTOSCOPE LOOPS

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

    ETUDE (MODEL NUMBERS 24A05 & 24A06)

    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

    INTERSTIM

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code EZW·March 7, 2013

    INVISALIGN SYSTEM

    FDA Adverse Event
    Other ·ALIGN TECHNOLOGY, INC.·Product code NXC·February 7, 2011

    PROTECTA XT DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·August 8, 2014

    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

    HF-RESECTION ELECTRODE, LOOP, 22.5 FR., 0.35 WIRE, 12°

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code KNS·August 11, 2016

    UNKNOWN

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