Product certification
Medical Devices
Medical devices are a heterogeneous category of products, such as active equipment, implants, reusable instruments, substances and materials, Sw, and more, intended for use on humans and therefore their safety and performance are of vital importance. To be put on the market and traded in EU, medical devices must comply with pertaining European legislations.
With a worldwide presence and a wide and in-depth experience in the medical field with several thousand certified devices in over 25 years of activity, Kiwa can provide complete and reliable information on the appropriate medical devices certification process to undertake, and deliver trusted conformity assessment activities and related services.
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