BEUDAMED
    14 results · 29ms · Sources: EU EUDAMED, US FDA

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    Magicore Narrow System

    FDA 510(k)
    FDA Class 2 ·Dental

    X-CORE

    FDA UDI
    Nuvasive, Inc.·00887517434296·X-CORE 2 Ti Core, Ø22x47-79mm

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112649·BARRON CORNEAL PUNCH 8.25MM

    PRIMED TRACHEOSTOMY TUBES (MULTIPLE)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BLADEWORKS MICROKERATOME BLADE, MODEL 7061

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    NA

    FDA UDI
    Zimmer, Inc.·00889024187870·

    STEIN PIN 3/32DX9LG ST5

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HTY·April 16, 2026

    1688 AIM 4K CAMERA HEAD WITH INTEGRATED COUPLER - INTERNATIONAL KIT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·September 13, 2024

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 31, 2008

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·August 12, 2011

    PROMOTE ACCEL CRT-D

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·July 11, 2013

    TPP THRUST PLATE 38      12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HRS·April 9, 2025

    FITMORE®, SHELL WITH SCREW CONES, UNCEMENTED, 48/GG

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 9, 2025

    ACCOLADE DR SL MRI (Model L311)

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