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

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    TurboHawk Plus Directional Atherectomy System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Spex

    FDA UDI
    SPEX LIMITED·09420051700918·Spex 2 Point Padded Hip Belt, Centre Pull, Side...

    Heinz Device

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215055851·

    Deltec

    FDA UDI
    ICU MEDICAL, INC.·00610586028468·

    MODIFICATION TO XIA SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARROW FLEXBLOCK CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VERSAJET

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW MEDICAL LTD·Product code FQH·June 4, 2025

    FARADRIVE¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DRA·August 1, 2025

    COBLATION

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code GEI·March 18, 2025

    COMPREHENSIVE LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·July 5, 2019

    EASYTOUCH

    FDA Adverse Event
    Malfunction ·BERPU MEDICAL TECHNOLOGY CO., LTD·Product code FMF·August 22, 2023

    MERCURY AMALGAM

    FDA Adverse Event
    Injury ·NA·Product code OIV·October 24, 2008

    ACCESS

    FDA Adverse Event
    Malfunction ·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·August 15, 2011

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·July 8, 2013

    TITA JET LIGHT II HP PUR KIT WITH 6.6F X 750 MM PRE-ATTACHED POLYURETHANE CATHET

    FDA Adverse Event
    Injury ·PFM MEDICAL MEPRO GMBH·Product code LJT·February 28, 2025

    TRUE METRIX

    FDA Adverse Event
    Injury ·TRIVIDIA HEALTH INC·Product code NBW·January 5, 2026

    JUGGERSTITCH CURVED IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·April 9, 2024

    TRUE METRIX AIR

    FDA Adverse Event
    Injury ·TRIVIDIA HEALTH INC·Product code NBW·March 6, 2026

    JUGGERKNOT 1.4MM SHRT W/NDLS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBI·July 3, 2024

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code KDJ·January 6, 2023