Veinplicity is CE Mark Certified!

Physeon is excited to announce that after four years of passionate research, development work and clinical studies our Veinplicity venous access device has passed its IS 13485 audit and received the CE certificationfor the European market! This means that Veinplicity can now be sold across the European Economic Zone and in any other country where the CE mark is accepted.

Certified as a Class IIA medical device, Veinplicity aids practitioners in gaining peripheral venous access in both adult and pediatric patients over the age of two.

With this news, our production line is in full swing and we are looking for distributors for this first-in-class, electrical stimulation device. If you are a medical device distributor, please contact to learn more about Veinplicity and the possibilities available to you.



The Veinplicity device is CE marked and registered as a Class IIa medical device in the European Union and as a Class II medical device in Canada. We are seeking FDA approval. The device is manufactured within the ISO 13485 standard in the United States.

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