BEUDAMED
    31 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 ×

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112885·CORNEAL TREPHINE BLADE6.75MM

    Responsive Arthroscopy Suture Anchor System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112724·BARRON VACUUM PUNCH 6.75MM

    SprintRay Apex Base - Light Pink - 1 Kg

    FDA UDI
    Sprintray, Inc.·00850039704659·APEX Base resin is a light-curable polymerizabl...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112823·BARRON VACUUM PUNCH 9.25MM

    ULTRASONIC NEBULIZER, MODEL NE-520

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    BLADDERSCAN BVI 6100

    FDA 510(k)
    FDA Class 2 ·Radiology

    BREATHING CIRCUIT SET, COAXIAL

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code BZO·March 5, 2026

    GE OEC 7600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 16, 2008

    SYSTEM 83 PLUS 9

    FDA Adverse Event
    Malfunction ·CUSTOM ULTRASONICS INC.·Product code FLG·June 28, 2013

    LAUREATE WORLD PHACO SYSTEM

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·August 5, 2011

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·September 3, 2025

    GORE® SEAMGUARD® BIOABSORBABLE STAPLE LINE REINFORCEMENT

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code FTM·November 9, 2021

    ENSEAL GENERIC PRODUCT CODE

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GEI·September 20, 2022

    UNKNOWN LAG SCREW

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·April 30, 2025

    HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP/DRIVELINE

    FDA Adverse Event
    Injury ·HEARTWARE, INC.·Product code DSQ·October 27, 2022

    VYPRO MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·March 24, 2022

    ENDURANT STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·February 23, 2022

    BD POSIFLUSH¿ PRE-FILLED SALINE SYRINGE

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·August 15, 2022

    SECURESTRAP UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GDW·May 18, 2021