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Clinical Trial Summary

The investigational product constitutes a medical device that is freely accessible to consumers and, as such, must be safe under real or reasonably foreseeable conditions of use and its safety must be tested before being placed on the market. Therefore, this study was designed to evaluate the biocompatibility of the experimental product, as provided for in legislation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05876546
Study type Interventional
Source Eurofarma Laboratorios S.A.
Contact Gleyce Lima
Phone 55 11 5090 8411
Email gleyce.lima@eurofarma.com
Status Not yet recruiting
Phase N/A
Start date May 30, 2024
Completion date August 30, 2024

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