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www.us-tech.com
October, 2021 ElEctronic Mfg SErvicES
Scanfil Supports Medtech Development from R&D to Market
By Michael Skinner, Editor M
edical technology and de- vice companies have unique requirements
when selecting a manufacturing partner. ISO-13485 medical de- vice certification is a must, but it’s only a baseline. It takes years for a contract manufacturer to devel- op accurate and precise processes, establish a network of suppliers for high-quality parts, and have the knowledge, resources, and ex- perience to ensure that products meet individual country and worldwide specifications and reg- ulations. Considerations for selec- tion include location, manufactur- ing capabilities, the breadth of services, quality, and a trustwor- thy team.
Rigorous Standards Medical manufacturing is
very well-established and there are many manufacturing firms —
Scanfil technicians evaluate a PCB at its factory in Sievi, Finland.
all with the same certificates and structure. What is important is not the complexity of the product being produced, because the same
regulatory system is used for all medical products. It’s finding the balance between filling regulato- ry system demands and having
the best efficiency, productivity, and cost-reduction model. Scanfil has been providing
manufacturing and system inte- gration services for more than 40 years for products that include communications network de- vices, automation system mod- ules, power and frequency con- verters, lift control systems, ana- lyzers, purifiers, slot and vend- ing machines, devices for meteor- ology, and much more. For the past 25 years, Scanfil
has also served companies devel- oping products for medtech, life science, and environmental meas- urement and analysis. Scanfil has 3,200 employees with nine facto- ries worldwide in North America, Europe, and Asia, and has its headquarters in Finland. These factories offer such services as engineering, develop-
Continued on next page
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