BEUDAMED
    107 results · 24ms · Sources: EU EUDAMED, US FDA

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    Surgical Face Masks

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112779·BARRON VACUUM PUNCH 8.0MM

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112632·BARRON CORNEAL PUNCH 8.0MM

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694094153·Screwdrivers Shaft, T8

    KAVO CORUND HANDPIECE 2013

    FDA 510(k)
    FDA Class 2 ·Dental

    KLARITY

    FDA 510(k)
    FDA Class 2 ·Radiology

    COMP RVRS SHLDR GLNSP STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·July 3, 2019

    FOOTPRINT PERIPHERALLY INSERTED CENTRAL CATHETER

    FDA Adverse Event
    Malfunction ·FOOTPRINT MEDICAL INC.·Product code LJS·May 18, 2026

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·November 27, 2024

    NEEDLE 25G 1IN

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FMI·November 26, 2024

    FIBERSTITCH IMPLANT, CURVED WITH TWO POLYESTER IMPLANTS AND 2-0 FIBERWIRE® SUTU

    FDA Adverse Event
    Malfunction ·T.A.G. MEDICAL PRODUCTS CORPORATION LTD·Product code MBI·August 19, 2024

    MONITORING ELECTRODES

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC.·Product code DRX·April 3, 2025

    MONITORING ELECTRODES

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH 200, LLC·Product code DRX·April 3, 2025

    GORE CARDIOFORM SEPTAL OCCLUDER

    FDA Adverse Event
    Malfunction ·W. L. GORE ASSOCIATES, INC.·Product code MLV·January 22, 2026

    BD NEXIVA NEARPORT 20GA X 1.00IN W/ MAXZERO

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·January 13, 2025

    BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 32 SIZE M

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 31, 2023

    GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/11 MM R E-CROSS

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·August 30, 2024

    CUP: MPACT ACETABULAR SHELL Ø48 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·May 8, 2024

    GMK-SPHERE 02.12.0510FR TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/10 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 10, 2023

    TR BAND

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DXC·October 3, 2025