BEUDAMED
    10,000 results · 55ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SCHUSTER ACETABULAR CUP FOR CEMENT/CEMENTLESS FIX.

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    ARC-2F ACETABULAR CUP

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORION BLADE PLATE FOR TIBIAL OSTEOTOMY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE EPI UNIPOLAR AND CAPSURE EPI BIPOLAR LEADS

    Scanlan® Surgical skin markers

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159029031·Scanlan® Surgical skin markers - Regular Tip, G...

    Devon

    FDA UDI
    Cardinal Health, Inc.·30884521049806·Surgical Site Mini-Marker

    Scanlan® PrepMARK

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159025392·Scanlan® PrepMARK - Reg Tip, Gentian Violet, No...

    EONS Nitrile Examination Gloves Powder Free

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE EPI

    System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

    FDA Pre-Market Approval
    FDA Class 3 ·Epi proColon

    System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

    FDA Pre-Market Approval
    FDA Class 3 ·Epi proColon

    System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

    FDA Pre-Market Approval
    FDA Class 3 ·Epi proColon

    System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

    FDA Pre-Market Approval
    FDA Class 3 ·Epi proColon

    System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

    FDA Pre-Market Approval
    FDA Class 3 ·Epi proColon

    System, Colorectal Neoplasia, Dna Methylation And Hemoglobin Detection

    FDA Pre-Market Approval
    FDA Class 3 ·Epi proColon

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE EPI

    EchoTip

    FDA UDI
    COOK IRELAND LTD·00827002492578·Echotip Ultra, Celiac Plexus Neurolysis Needle

    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·EPi-Sense®, EPi-Sense ST™ Guided Coagulation System

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·EON MINI LE CHARGER, EON MINI LE CHARGING SYSTEM

    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

    FDA Pre-Market Approval
    FDA Class 3 ·EPi-Sense and EPi-Sense ST Guided Coagulation System