From idea to medical device

FAST. STRUCTURED. CERTIFIED.
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Your MedTech project is in good hands

TECHNICAL DEVELOPMENT WITH RESPONSIBILITY

Single-use sterile products and implants require the highest demands on design, material selection, functionality, and documentation. At OSCOMED, we support you precisely where it matters most: in the early stages of product development.

Whether it's an initial sketch or a concrete concept – we develop your component or complete solution in a structured, regulatory-compliant manner, with one clear goal: to transform your idea quickly and precisely into a verifiable product.

Technical expertise meets industry understanding

WHAT WE DO FOR YOU

Our customers benefit from an interdisciplinary development approach that considers technology, manufacturing, and regulatory approval from the outset.

  • Product development for single-use sterile products and implants
  • Materials consulting: selection of biocompatible polymers, thermoplastics, and silicones
  • Plastic-compatible design and tooling with a focus on function, tolerances, and series production capability
  • Design and process FMEAs, risk analyses, and design verification
  • Documentation according to ISO 13485 and MDR/FDA
  • Feasibility studies and tooling concepts
  • Technical project management with dedicated contacts

Speed as a system

TIME-TO-MARKET MATTERS

We understand the importance of speed in medical technology – especially for new product generations and innovation projects. Thanks to our in-house development resources, integrated toolmaking, and streamlined processes, we can complete even complex projects quickly.

  • Fast quotation phase & technical consultation
  • In-house design & project management
  • Short paths to prototyping and 3D printing
  • In-house toolmaking & production
  • Project start often possible within a few days

Understand what you need

WE ARE LISTENING

Good technical solutions start with good communication. That is why we focus on an open understanding of the project, active listening and joint decisions. Your requirements form the basis for our actions – technically, economically and personally.

  • Personal project support from our expert engineers
  • Regular status updates and clear roadmaps
  • Documented coordination and change tracking
  • Early involvement of Quality Management, Regulatory Affairs, and Manufacturing

What we develop is practicable

Ready for licensing & series production
Our developments are not only impressive in CAD – they also prove themselves in practice. All concepts are geared towards series production and regulatory compliance.
  • ISO 13485-compliant development documentation
  • Support with MDR & FDA approval processes
  • Consideration of sterilisation, packaging & biocompatibility
  • Transition to production & process validations from a single source

Our development expertise in practice

TYPICAL AREAS OF APPLICATION
  • Catheter systems and single-use sterile products
  • Flexible connectors and tubing adapters
  • Polymer implant components
  • Components for diagnostics and interventional procedures
  • Functional components for OEM products