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Brazil

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Brazil
Medical Device Product Registration and Approval

MEDICAL DEVICE REGULATION IN BRAZIL


Medical devices are regulated by the Brazilian Health Regulatory Agency (ANVISA) from the Ministry of Health in Brazil. Its primary objective is to protect and promote public health by exercising health surveillance over products and services and this includes any processes, ingredients, and/or technologies that may pose any health risk. Medical devices are regulated under Law No 6,360.


MEDICAL DEVICE REGISTRATION AND APPROVAL IN BRAZIL


Medical devices are classified into class I, II, III and IV (I being the lowest risk and IV being the highest risk).


There are 2 registration routes in Brazil; Cadastro registration route for the lower risk devices, and Registro registration route for the higher risk device. The significant difference between the 2 routes, is that the higher risk device requires a more detailed information from the technical file and it includes the Clinical Evaluation.

Example Of Approval

Source: ANVISA

Medical device regulatory guidelines
Product Registration
License Holding
Extra RA/QA Suppprt
License Holding

LATIN AMERICA REP

Foreign manufacturers must appoint an US agent as a local point of contact with US FDA.

If you are a foreign manufacturer, you may appoint ARQon to act as your authorized representative in the US.


Some of the responsibilities include:

  • Acting as a first point of contact with Regulatory authorities and import/customs offices

  • Being responsible for pre-certification and post-approval inquiries

  • Liaising between the Medical Device authority and foreign manufacturer in incident of Field Safety Corrective Action (FSCA), serious adverse event reporting to competent authorities, and in cooperation with manufacturer’s distributor

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Extra RA/QA Support

MONTHLY REGULATORY SUPPORT FOR REGIONAL REGISTRATION

ARQon provide onsite/offsite monthly regulatory support for regional registration in Brazil.


Contact Us for more details.

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Drug Services
Drug Services

THERAPEUTIC AND COSMETIC APPROVAL

ARQon provides therapeutic and cosmetic approval for Drug, Cell Tissue, Traditional Medicine, Health Supplements and Cosmetic in Brazil.


Read more

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Health Safety
Health Safety

WIRELESS, RADIATION AND PACKAGING APPROVAL

ARQon provides Wireless, Radiation, Packaging and Non-medical Device Approval in Brazil.


Contact Us for more details.

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Precisa de mais detalhes? Contate-nos. 

Estamos aqui para ajudar. Contacte-nos na Plataforma ATTOPOLIS.

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