BEUDAMED
    4,988 results · 43ms · Sources: EU EUDAMED, US FDA

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014604831·BERCHTOLD B810, B710 3" DELUXE

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·Tupoa LV/ATX & Kronos LV-T / CRT-D & Corox OWT Steroid LV Pacing Lead

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·TUPOS LV/ATX & KRONOS LV-T CRT-D & COROX OWT STEROID LV PACING LEAD

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·Tupos LV/ATX & Kronos LV-T CRT-D and Corox OWT Steroid LV Pacing Lead

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·Tupos LV/ATX & Kronos LV-T CRT-D & Corox OWT Steroid LV Pacing Lead

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·Tupos LV/ATX & Kronos LV-T CRT-D & Corox OWT Steroid LV Pacing Lead

    Stimulator, Ultrasound And Muscle, For Use Other Than Applying Therapeutic Deep

    FDA Pre-Market Approval
    FDA Class 3 ·SONIC ACCELERATED FRACTURE HEALING SYSTEM MODEL 2A

    Addenbrooke/Owa Grommet

    Basic UDI-DI
    EU MDD · Eu Md Class 2b ·Exmoor Plastics Limited·1 device

    Barrier, Absorbable, Adhesion

    FDA Pre-Market Approval
    FDA Class 3 ·ADEPT Adhesion Reduction Solution

    AMPLATZER TorqVue 45x45 Delivery Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BD Intraosseous Infusion System

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Wózek zabiegowy FWZ-1

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Formed Pro Spółka z Ograniczoną Odpowiedzialnością ·4 devices

    Sentimag System, Sentimark Magnetic Marker Systerm

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    IP85092: Sterile, Single Use, CONVERTEERBAK OOZ

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·HASA OPTIX·1 device

    IP85095: Sterile, Single Use, CHALAZION SET OOZ

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·HASA OPTIX·1 device

    IP85092 x10: Sterile, Single Use, CONVERTEERBAK OOZ

    Basic UDI-DI
    EU MDD · Eu Md Class 2a ·HASA OPTIX·1 device