Veinplicity hosts its first training session

Physeon wants to provide medical representatives with all the tools and knowledge necessary to successfully enter the venous access market. To do this, we offer complete training modules on the Veinplicity™ device for our partners’ medical representatives and product managers. This includes in-depth information on the Veinplicity device works, its studies, material on venous access and failure rates, tips on messaging and promotion, and much more.

In light of our upcoming launch in the UK and Ireland, Physeon completed its first training session with LINC Medical, our UK/Ireland distribution partner.

As you can see below, it was a very interesting and busy day!

#Distributors #training #branding


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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