EUROLAB laboratory provides testing and compliance services within the scope of ISO 25539-3 standard. ISO 25539-3 specifies requirements for vena cava filters based on available medical information.
Regarding safety, it gives requirements for intended performance, design features, materials, design evaluation, manufacturing, sterilization, packaging, and information provided by the manufacturer. ISO 25539-3 supplements ISO 14630, which specifies general requirements for the performance of inactive surgical implants.
The following are outside the scope of ISO 25539-3:
EUROLAB assists manufacturers with ISO 25539-3 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
To get an appointment, to get more detailed information or to request an evaluation, you can ask us to fill in our form and reach you.