BEUDAMED
    24 results · 21ms · Sources: EU EUDAMED, US FDA

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    ARTHREX MENISCAL DART, ARTHREX MENISCAL DARTSTICK, ARTHREX CHONDRAL DART

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K082959

    FDA UDI
    Unimed Medical Supplies, Inc.·06945664812412·SpO2 interface cable/Philips-Masimo/2.2M/309+12...

    Unimed

    FDA UDI
    Unimed Medical Supplies, Inc.·06936735463947·One-piece ECG Monitor Cable Philips

    MetaSystems Probes

    FDA UDI
    MetaSystems Probes GmbH·04251315807198·XL BCR/ABL1/ASS, 10x 100µl, Deletion Probe/Dual...

    CARTO XP SYSTEM

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, LTD·Product code DQK·November 30, 2007

    CARTO XP EP NAVIGATION SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER, LTD (HAIFA, ISRAEL)·Product code DQK·August 14, 2008

    TRIAGE TOX DRUG SCREEN CONTROLS, CATALOG #94001

    FDA 510(k)
    FDA Class 1 ·Clinical Toxicology

    GRAMS POLYPROPYLENE NONABSORBABLE SUTURE

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

    CARTO XP EP NAVIGATION SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER LTD. (HAIFA, ISREAL)·Product code DQK·April 17, 2008

    DELTA CER FM HD 036/-4MM 12/14

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 23, 2026

    PALMAZ BLUE .014 PERIPHERAL STENT SYSTEM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code FGE·April 29, 2013

    ALARIS PUMP

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code FRN·May 4, 2011

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·July 28, 2008

    UNKNOWN AVANTAGE HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·March 6, 2025

    BIOLOX DELTA CERAMIC FEMORAL HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·March 2, 2017

    32MM COCR BIOMET FEM HD -3 NK

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·April 30, 2025

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·December 19, 2023

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·November 10, 2021

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·August 3, 2022

    CARTO® 3 SYSTEM

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·February 16, 2023