Wellcome to FEA WORKS! 

On the one hand, you receive services for the application of the Finite Element Method (FEM) in all areas of development, research and industry.

We work on engineering problems for you from the fields of statics , dynamics , thermodynamics and fluid mechanics . FEM calculations, proof of strength , lifetime proof , proof of screws , rivets and welds as well as component optimization and CFD analyzes are our daily business.

On the other hand, you get finished stent designs or stent models for download free of charge.These models are tested and designed according to standard and may be further processed.

We creatively develop stent models and medical implants and provide you with this stent models database free of charge. You may download our models and process them for your own purposes. If you want to know more about the subject, feel free to contact us.

The following international standards and regulations serve as a basis for stent designs and the corresponding proofs and fatigue tests :

ISO 25539-1: Cardiovascular implants – Endovascular devices – Part 1: Endovascular prostheses

ISO 25539-2: Cardiovascular implants – Endovascular devices – Part 2: Vascular stents

ISO 25539-3: Cardiovascular implants – Endovascular devices – Part 3: Vena cava filters

ASTM F2514: Finite Element Analysis (FEA) of Metallic Vascular Stents Subjected to Uniform Radial Loading

ASTM F2477: Standard Test Methods for in vitro Pulsatile Durability Testing of Vascular Stents

ASTM F2942: Standard Guide for in vitro Axial, Bending, and Torsional Durability Testing of Vascular Stents

ASTM F3067: Guide for Radial Loading of Balloon Expandable and Self Expanding Vascular Stents

ASTM F2079: Elastic Recoil of Balloon-Expandable Stents

ASTM F3211: Fatigue-to-Fracture (FtF) Methodology for Cardiovascular Medical Devices.

FDA Guidance for Industry and FDA Staff: Non-Clinical Engineering Tests and Recommended Labeling for Intravascular Stents and Associated Delivery Systems. April 18, 2010

FDA Guidance for Industry and FDA Staff: Reporting of Computational Modeling Studies in Medical Device Submissions. September 21, 2016

Heart Valves:

ISO 5840-3: Cardiovascular implants – Cardiac valve prostheses – Part 3: Heart valve substitutes implanted by transcatheter techniques

ISO 5910: Cardiovascular implants and extracorporeal systems – Cardiac valve repair devices

We offer a comprehensive range of FEA engineering and simulation, consulting and FEA know-how, product designs (eg stent designs) from the conceptual phase to the finished product. Our services are cost effective and we provide professional FEA solutions.

The following standards and regulations serve as the basis for the strength analysis and strength proofs:

EuroCode 1, EuroCode 3, EuroCode 9, DIN 18800,

FKM guideline,

DIN EN 12663, DIN EN 61373, GM / RT2100, BS 7608,

DIN EN 15085, DVS 1608, DVS 1612,

DIN 15018, DIN EN 13001, EN 13155,

VDI 2230, DIN 25201,

AS 1210, Pressure Equipment Directive, AD 2000 - Fact Sheets