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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    da Vinci Xi Surgical System, da Vinci X Surgical System

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

    Dandy Clear Aligners

    FDA UDI
    Orthly, Inc.·00860006891206·

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668109045·CAPSULE STAINING CANNULA 25GA

    BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP

    FDA 510(k)
    FDA Class 2 ·Dental

    INNERCHANGE MICRO-INTRODUCER CATHETER, MODELS 7900, 7901, 7902, 7903, 7904 AND 7905

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    8CH INFINITY DBS FLEX EXTN KIT, 60CM, B

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code MHY·September 16, 2022

    TRUWAVE, VAMP

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·March 20, 2025

    MITRACLIP SYSTEM STEERABLE GUIDE CATHETER

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code DRA·October 15, 2014

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 17, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 23, 2011

    TRUWAVE, VAMP

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES DR·Product code KRA·April 18, 2025

    TRUWAVE, VAMP

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES DR·Product code DXO·March 20, 2025

    NV EHXL ALIP LNR G4 36MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 18, 2022