DERMADRY LABORATORIES INC.

Dermadry Laboratories Inc. produces a range of iontophoresis devices aimed at treating hyperhidrosis. Their lineup includes a controller unit, various electrode sets for hands, feet, and underarms, cables, portable cases, and even towels for use with the system. Each component is designed to work together to deliver the iontophoresis therapy.

The company is based in Canada, as indicated by the country code CA. Its iontophoresis devices are listed in the European Union’s Eudamed database, which is the central repository for medical device information across the EU. This listing shows that the products have been entered into the official regulatory system.

According to the provided data, Dermadry’s devices fall into two risk categories: Class I and Class IIa. Class I covers lower‑risk devices, while Class IIa includes devices with a moderate level of risk that require a higher level of conformity assessment before they can be placed on the market.

Yes, the data mentions several product variants that carry multilingual labeling—English, French, German, Spanish, Italian, and Dutch—specifically for the European market. These versions, such as the underarm electrodes and hands‑and‑feet kits, are packaged to meet language requirements across EU member states.

A complete Dermadry system typically comprises a controller that generates the electrical current, interchangeable electrodes for hands, feet, and underarms, connecting cables, a portable case for storage, and disposable towels to facilitate treatment. Together, these parts enable users to perform iontophoresis therapy at home.