BEUDAMED
    224 results · 22ms · Sources: EU EUDAMED, US FDA

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    MANUKATEX

    FDA 510(k)
    FDA Unclassified ·Unknown

    Corin BiPolar-i

    FDA UDI
    CORIN LTD·05056139233883·Acetabular Trial Ø42

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694055192·6mm Ring Curette

    Sapphire 1100 42

    FDA UDI
    SIZEWISE RENTALS, L.L.C.·00845699000975·

    VADI MEDICAL

    FDA UDI
    VADI MEDICAL TECHNOLOGY CO., LTD.·04719894389196·Airway Connector

    DIFUSION TECHNOLOGIES XIPHOS INTERBODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CT PERFUSION 2

    FDA 510(k)
    FDA Class 2 ·Radiology

    ANCHOR BOLT-LSB STYLE

    FDA Adverse Event
    Malfunction ·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GCZ·April 18, 2018

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024636842·

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024636835·

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024360310·

    Trilogy®

    FDA UDI
    Zimmer, Inc.·00889024360303·

    OSCOR ADELANTE BREEZEWAY 10F C120¿ S79CM D84CM Catalog # AB101078 Is designed to facilitate the introduction of catheters to any of the heart chambers, including the left atrium via a transseptal puncture.

    FDA Enforcement
    Class II ·Terminated·Oscor, Inc.·December 28, 2016

    POWER CORD, TGS SYSTEM V2, 20' LG

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·October 8, 2019

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·May 13, 2013

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·September 23, 2014

    CARENDO

    FDA Adverse Event
    Other ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·May 26, 2011

    BD PLASTIPAK¿ 50ML CONCENTRIC LUER LOCK SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·January 14, 2022

    VAPR3 FOOTSWITCH *EA

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HRX·January 11, 2021

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·SUBCUTANEOUS IMPLANTABLE DEFIBRILLATOR (S-ICD) SYSTEM