BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    ELECTROSUGRICAL RESECTION AND VAPORIZATION ELECTRODE SERIES

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

    HF-RESECTION ELECTRODE, FOR TURIS

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·February 9, 2023

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024

    HF-RESECTION ELECTRODE, LOOP

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·March 28, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·December 28, 2022

    HF-RESECTION ELECTRODE, LOOP

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·April 27, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 21, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 21, 2023

    HF-RESECTION ELECTRODE, ROLLER

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·April 28, 2023

    ATLANTIS® Anterior Cervical Plate System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994235176·SCREW 3120418 4.0 X 18 SELF DRILL FIX

    Unity Total Knee System

    FDA UDI
    CORIN LTD·05056139243950·UNITY KNEE™ PS-C INSERT - Size 4 x 18mm

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613154156160·BONE SCREW, CROSS-PIN, SELF-TAPPING

    APEX PS Knee

    FDA UDI
    Omni Life Science, Inc.·00841690113263·PS Insert, Size 4 x 18mm

    Viper

    FDA UDI
    DIVERSATEK HEALTHCARE, INC.·00816734021736·Fixed Wire Balloon Dilator

    GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SUPERIOR STARBURST REUSABLE SELF-ADHERING TENS/NMES/FES STIMULATING ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    KING SEPTEMS

    FDA Adverse Event
    Malfunction ·KING SEPTEMS·Product code LMA·November 1, 2012

    IOLMASTER 500

    FDA Adverse Event
    Malfunction ·CARL ZEISS MEDITEC AG (JENA)·Product code HJO·October 14, 2015

    X3 TRIATHLON INSERT PS#7 16MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·May 20, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 26, 2014