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

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    Cone Tip Ureteral Catheter, Rutner Universal Wedge Catheter

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

    Orbit Depressor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100899·SCHEPENS SCLERAL DEPRESSOR MEDIUM

    AED

    FDA UDI
    NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.·00848657018975·Meniscotome sharp and hard cutting edge

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100790·FLIERINGA FIXATION RING 18MM

    Rongeur

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108529·BEYER RONGEUR SINGLE ACTION

    INION SPINAL GRAFT CONTAINMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    3DHJD CAMERA SYSTEM MODEL

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

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·June 12, 2025

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 15, 2014

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 23, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 22, 2011

    LATITUDE ELBOW ANATOMIC HUMERAL SPOOL SZ PETIT+ SIDE DROIT

    FDA Adverse Event
    Injury ·TORNIER INC·Product code JDB·September 20, 2024

    INTELLIVUE MULTI-MEASUREMENT MODULE X3

    FDA Adverse Event
    Malfunction ·PHILIPS MEDIZIN SYSTEME BÖBLINGEN GMBH·Product code MHX·February 11, 2026

    RING TRANSJUGULAR INTRAHEPATIC ACCESS SET

    FDA Adverse Event
    Malfunction ·COOK INC·Product code DYB·November 15, 2019

    Ingenia 3.0T-a Magnetic Resonance Medical Electrical Systems indicated for use as a diagnostic device. The system can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the head, body, or extremities Models: 781342 781377

    FDA Enforcement
    Class II ·Completed·Philips North America Llc·September 15, 2021