BEUDAMED
    10,000 results · 126ms · 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.

    SCM CATH ( SIZES ARE VARYING BETWEEN 16G X 2'' AND 24G X 3/4'' ), MODEL 1.50, 1.77,1.88',2, 1.25, 1.50, 1.77,

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Prostate-Specific Antigen (Psa) For Management Of Prostate Cancers

    FDA Pre-Market Approval
    FDA Class 2 ·ACS:180(TM)/ADVIA CENTAUR(TM) PSA ASSAY

    hot cold pack

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Anhui Kamt Ice Pack Co.,Ltd.·17 devices

    Extracorporeal Shock Wave Lithotripter (U200)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PVC SMOOTH BIRE TUBING WITH DOUBLE SWIVEL ELBOW

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·Morton Medikal San ve Tic A.Ş.·1 device

    Merck Healthcare KGaA

    Authorized representative
    🇩🇪 Germany·1 Manufacturer·47 Devices

    Fidelity 25 Alginate

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Davis Schottlander & Davis Ltd·1 device

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·RESOLUTE INTEGRITY ZOTAROLIMUS ELUTING CORONARY STENT SYSTEM

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·ENDEAVOR SPRINT ZOTAROLIMUS-ELUTING CORONARY STENT SYSTEM

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·INTEGRITY CORONARY STENT SYSTEMS

    Implant, Cochlear

    FDA Pre-Market Approval
    FDA Class 3 ·NUCLEUS 24 COCHLEAR IMPLANT SYSTEM

    VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left

    FDA 510(k)
    FDA Class 2 ·Neurology

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·HeartSync Multifunction Disposable Single-Use AED Defibrillator Pads

    Synergy Health Westport Ltd

    FDA registration
    Synergy Health Westport Ltd·1 product·🇮🇪 Ireland

    Trinity Biotech

    FDA registration
    TRINITY BIOTECH, PLC·1 product·🇮🇪 Ireland

    Synergy Health Westport Ltd

    FDA registration
    Synergy Health Westport Ltd·2 products·🇮🇪 Ireland

    FOR CLINICAL USE (MULTIPLE BRANDS)

    FDA registration
    DEPUY (IRELAND)·1 product·🇮🇪 Ireland

    Integra LICOX PT02 Monitor

    FDA registration
    INTEGRA LIFESCIENCES (IRELAND) LIMITED·1 product·🇮🇪 Ireland

    Boston Scientific Limited

    FDA registration
    Boston Scientific Limited·1 product·🇮🇪 Ireland

    Boston Scientific Limited

    FDA registration
    Boston Scientific Limited·1 product·🇮🇪 Ireland