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Take the User Survey:

Select the product line and fill out the form

Vision Care

This Survey aims to evaluate the clinical performance and safety of Mediphacos products that are on the market.

Target audience: Ophthalmologists who use intraocular lenses, Keraring, contact lenses and Medilon.

This survey does not aim to assess satisfaction with the equipment or services provided by Mediphacos.

Time to complete a User Survey: Less than 3 minutes.

Post-market monitoring is a mandatory activity for manufacturers of health products in compliance with national and international standards, such as:

MEDDEV 2.12/2 Rev. 2, 2012 - Post Market Clinical Follow-Up Studies.

MEDDEV 2.12/1 Rev. 8, 2013 - Guidelines on Medical Devices Vigilance System.

MDR 2017/745 - Regulation 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC.

EN ISO 13485:2016 - Medical devices - Quality management systems - Requirements for regulatory purposes.

Resolução da ANVISA RDC Nº 67, 2009 - Dispõe sobre normas de tecnovigilância aplicáveis aos detentores de registro de produtos para saúde no Brasil.