In accordance with the RDC No. 751 of 2022 established by ANVISA, we make the instructions for use of the products available for download.
To consult the revision of the instructions for use relating to the manufacture of the product, the user must check the date of manufacture contained in the product labeling and download the latest version prior to the date of manufacture.
To obtain the printed instructions for use free of charge for display and shipment, please contact our customer service by clicking here. Click here
Kit Dilatador para Neuroendoview Plus Traumec Rev.00 - Anvisa Registration No. 80455630076
Kit Dilatador para Neuroendoview Plus Traumec Rev.01 - Anvisa Registration No. 80455630076
Kit Dilatador para Neuroendoview Plus Traumec Rev.02 - Anvisa Registration No. 80455630076
Kit Dilatador para Neuroendoview Plus Traumec Rev.03 - Anvisa Registration No. 80455630076
Kit Dilatador para Neuroendoview Plus Traumec Rev.04 - Anvisa Registration No. 80455630076
Kit Dilatador para NeuroEndoview Plus Traumec Rev.05 - Anvisa Registration No. 80455630076
- TRAUMEC TECNOLOGIA E IMPLANTES ORTOPÉDICOS
- +55 19 3522-1177
- Rua 1CA, n° 202 – Cidade Azul II – Rio Claro (SP)
- CEP: 13505-820 - Brasil
© 2023 Traumec Health Technology - Todos os direitos reservados - Imagens meramente ilustrativas
