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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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CONTACT

 

E: info@physeon.com
T: +41 52 630 70 80

ADDRESS

 

Physeon GmbH

Herrenacker 15

8200 Schaffhausen

Switzerland

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