The Jansen Medicars Testing Process
At Jansen Medicars, the safety and quality of our products are our top priorities. To ensure that every product meets the highest standards and expectations, we use a comprehensive and advanced testing process.
Simulations During the Design Process
The testing process begins as early as the design phase, where we use our own simulation testing environment. This advanced technology allows us to virtually simulate the stability of a product. By testing the product on various aspects, we can accurately calculate whether it meets the stability requirements. These simulations help us identify and adjust potential weak points at an early stage.
From Simulation to Practice: The Extensive Tests in Our Test Center
After manufacturing, our products undergo a second testing phase in our experience center. The products are tested here in accordance with the IEC60601-1 standard. This international standard for medical electrical equipment sets strict requirements for the safety and performance of medical products. Our tests include:
- Tilt tests: The product is subjected to different angles and positions to check whether it remains stable and does not tip over.
- Glide tests: These tests simulate situations in which the product is moved over different surfaces to ensure that it moves smoothly and safely without unexpected shifts.
- Driving tests: During these tests, the product is moved on various surfaces and at different speeds to ensure maneuverability and stability during transport.
- Threshold tests: In these tests, we check how the product moves over thresholds and other obstacles to ensure that it remains safe and stable when used in a dynamic hospital environment.
Our test center also offers the possibility of making video recordings. This way, you can also analyze the tests yourself from a distance. In addition to stability tests, we also perform ergonomics tests. In our OR simulation test room, our customers can extensively test the products in various setups. Through these extensive tests, we ensure that our products not only meet the legal standards, but also the expectations of our customers.
MDR Class 1 Registration
All products we produce, including custom-made products, are registered as MDR Class 1 (CE marking). This means that our products comply with the strict requirements of the European Union's Medical Device Regulation (MDR), which ensures the safety and performance of medical devices. The MDR Class 1 registration demonstrates that our products are safe to use and comply with all relevant legal requirements.
At Jansen Medicars, we take our responsibility for the quality and safety of our products very seriously. By using advanced AI simulations and extensive practical tests, we ensure that every product meets the highest standards. Our commitment to innovation and reliability makes us a trusted partner in the healthcare sector.
Bron: Jansen Medicars
