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Thermal Management of Electro-mechanical Devices |
Fluid Flow Simulation for Pumps and Hydraulic systems |
Actuation System - Kinematic synthesis and analysis |
Optimization of Design for Fit, Form and Function |
Drop Test validation |
Hot & Cold Chamber Test Simulation |
Dimensional Management - Effect on Operational safety |
Life Estimation - meet Warranty requirements |
Sealing System - Elastomeric seal analysis |
Plastic snap-fit design validation |
Compliance checking to FDA, CE and other standards |
Estimation of forces in actuation, assembly and operation |
Noise, Vibration and Durability Analysis of devices and components |
Prediction of Failure Modes and Effects |
For Medical Devices, Failure is not an option. Critical Life Support
systems, Patient Welfare devices, Supplementary Equipments, Operaating Theatre Equipments
and devices are intended to perform all the time without reprieve. It is important
that the designs are fail-safe. Compelling reasons to perform FEA as a part
of Design Validation include: