BEUDAMED
    1,403 results · 23ms · Sources: EU EUDAMED, US FDA

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    Probe Cover: JZ-KBT-001, JZ-KBT-002, JZ-KBT-005, JZ-KBT-007, JZ-KBT-008, JZ-KBT-009, JZ-KBT-010, JZ-KBT-015, JZ-KBT-025, JZ-KBT-026

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OSE

    FDA UDI
    ORTHODONTIC SUPPLY & EQUIPMENT COMPANY INC·00810042124769·EXPANDO RETRACTOR - LARGE #3

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193113418·HA PEEK EVOS Straight, ,9mmx8mmx 30mm , FLAT 0...

    NA

    FDA UDI
    Stryker GmbH·07613154639724·Screw Marker 20,9

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112526·BARRON VACUUM TREPHINE 8.25MM

    A-CIFT® SoloFuse®

    FDA UDI
    SPINEFRONTIER, INC.·00190361023692·A-CIFT SOLOFUSE IBFD, Lordotic 13mm Long, 17mm ...

    HP M2376A DEVICE LINK SYSTEM, MODEL M2376A

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3I IMPLANTS; OSSEOTITE DENTAL IMPLANTS; OSSEOTITE NT DENTAL IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Dental

    TOSCA 500 PCO2, SPO2 AND PULSE RATE MONITORING SYSTEM, MODEL 5202009

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

    FDA Adverse Event
    Malfunction ·Product code LWS·August 12, 2023

    ABL800 FLEX

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·April 21, 2020

    LCS COMPLETE M/B PAT CEM STD

    FDA Adverse Event
    Injury ·9616671 DEPUY (IRELAND)·Product code NJL·October 27, 2014

    LAUREATE WORLD PHACO SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 27, 2013

    UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code JGS·August 5, 2011

    INRATIO

    FDA Adverse Event
    Malfunction ·BIOSITE INCORPORATED·Product code JPA·April 15, 2009

    BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM

    FDA Adverse Event
    Malfunction ·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code QJR·March 19, 2021

    ENPATH MYOPORE SUTURELESS MYOCARDIAL PACING LEAD

    FDA Adverse Event
    Malfunction ·GREATBATCH MEDICAL·Product code DTB·August 12, 2023

    ACRYSOF RESTOR

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code MFK·April 17, 2009

    640G INSULIN PUMP MMT-1711K

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·April 11, 2022

    MOBILE INFANT WARMER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code FMT·November 9, 2010