BEUDAMED
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    SPRINT QUATTRO SECURE S™ DXAC/DSP

    FDA UDI
    MEDTRONIC, INC.·00643169535923·LEAD 693575 SPRINT US SI MCRD

    SPRINT QUATTRO SECURE S™ DXAC/DSP

    FDA UDI
    MEDTRONIC, INC.·00643169535930·LEAD 6935100 SPRINT US SI MCRD

    QIAsymphony® DSP Virus/Pathogen Midi Kit

    FDA UDI
    QIAGEN GmbH·04053228045786·

    Sprint Quattro Secure S™ DXAC/DSP

    FDA UDI
    MEDTRONIC, INC.·00613994446114·LEAD 693575 US EN SI MCRD

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·THERASCREEN EGFR RGQ PCR KIT

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·THERASCREEN KRAS RGQ PCR KIT

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Durata, Optisure

    Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·Isoflex

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·Quickflex µ, Quartet

    SONIC INNOVATIONS COMPLETELY-IN-THE-CANAL DSP HEARING AID WITH SOFT SHELL

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Permanent Defibrillator Electrodes

    FDA Pre-Market Approval
    FDA Class 3 ·CAPSURE SENSE LEAD

    DSP for cobas 8100

    Basic UDI-DI
    EU IVDR · Eu Ivd Class A ·Hitachi High-Tech Corporation·1 device

    Monitor, Skin Resistance/Skin Temperature, For Insulin Reactions

    FDA Pre-Market Approval
    FDA Class 3 ·SLEEP SENTRY

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·ENDOTAK(R) LEAD SYSTEM

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC ARRHYTHMIA MANAGEMENT DEVICES INCLUDING MODEL 7221B/CX/D/E MICRO JEWEL DEVICE USED WITH CPI ENDOTAK

    CARDIOSAVE HYBRID INTRA-AORTIC BALLOON PUMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTRA-AORTIC BALLOON FOR OPTIONAL SHEATHLESS INSERTION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    10.5 FRENCH PERCUTANEOUS DOUBLE LUMEN INTRA-AORTIC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PERCUTANEOUS INTRA-AORTIC BALLOON CATHETERS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DATASCOPE 8.5 FRENCH ELECTRODE INTRA-AORTIC BALLOO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular