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If you are struggling to get any cancer-related information then feel free to contact us and let us know. Our medical team will answer your query as immediately as possible.
CANKADO is approved as an active Class I medical device within the European Union (registration number DE/CA59/11976/2017) and is compliant with the FDA classification for Mobile Medical Devices (2015) Appendix B.
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CANKADO’s PRO-react Onco helps efficient patient physician communication in the treatment phase.
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CANKADO is approved as an active Class I medical device within the European Union (registration number DE/CA59/11976/2017) and is compliant with the FDA classification for Mobile Medical Devices (2015) Appendix B.