BEUDAMED
    63 results · 17ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (4F)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (4F)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (4F)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (6F)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (4F, 1.5-4.5mm)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (6F)

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (6F)

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Artificial Iris

    FDA Pre-Market Approval
    FDA Class 3 ·CustomFlex Artificial Iris

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (6F)

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (6F)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (6F)

    Scaffold, Dissection Repair

    FDA Pre-Market Approval
    FDA Class 3 ·Tack Endovascular System (4F, 1.5-4.5mm)

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·AORTIC VALVULOPLASTY BALLOON DILATATION CATHETER

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·BOSTON SCITNTIFIC SCIMED AORTIC VALVULOPLASTY(TM) CATHETER

    Artificial Iris

    FDA Pre-Market Approval
    FDA Class 3 ·CustomFlex Artificial Iris

    Pulse-Generator, Program Module

    FDA Pre-Market Approval
    FDA Class 3 ·MANSFIELD SCI. AORTIC VALVULOPLASTY CATHETER