BEUDAMED
    27 results · 25ms · Sources: EU EUDAMED, US FDA

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    CD HORIZON ECLIPSE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PowerPICC Provena Sherlock 3CG

    FDA UDI
    Bard Access Systems, Inc.·00801741228544·Catheter Placement Kit

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001066·artVeneer life upper anteriors, CL, A3

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369085·DOUBLE CLAMP BAR 35 INCHES

    N/A

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369092·OFFSET DOUBLE CLAMP BAR 35 INCHES

    SYNTHES (USA) LOCKING CONDYLAR PLATE (LCP) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNTHETIC (WHITE) VINAL POWDERED PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MultiPolar®

    FDA UDI
    Zimmer, Inc.·00889024115729·

    DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code PQF·May 16, 2019

    OFFSET DOUBLE CLAMP BAR

    FDA Adverse Event
    Malfunction ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code HST·June 12, 2009

    OFFSET DOUBLE CLAMP BAR

    FDA Adverse Event
    Malfunction ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code HST·June 12, 2009

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

    ACCESS® 2 IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·February 24, 2011

    LEAD MODEL 302

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 22, 2008

    OFFSET DOUBLE CLAMP BAR

    FDA Adverse Event
    Malfunction ·ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS·Product code HST·June 12, 2009

    SPINALPAK ASSEMBLY

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·October 30, 2020

    SPINALPAK ASSEMBLY

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·November 12, 2020

    BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·June 11, 2024

    BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·October 25, 2023

    BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATOR SYSTEM

    FDA Adverse Event
    Injury ·EBI, LLC.·Product code LOF·November 7, 2024