Medtech projects require careful material decisions, robust documentation and early manufacturability validation. We support COC, COP, PC, PA, PEEK and PSU selection, ISO 10993, USP Class VI and FDA 21 CFR requirements, and prototypes that closely reflect series production.
Project risks become visible through workshops, DFM reviews and sampling phases, creating solid decisions for material, tooling, suppliers and quality.
How We Support
- Material selection based on function, standards, cost and availability.
- Prototypes and additively manufactured tooling for fast testing.
- Sampling, process window and documentation through release.