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 Instrumental CMF Traumec Rev.00 - Anvisa Registration No. 80455630104
Kit Instrumental CMF Traumec Rev.01 - Anvisa Registration No. 80455630104
Kit Instrumental CMF Traumec Rev.02 - Anvisa Registration No. 80455630104
Kit Instrumental CMF Traumec Rev.03 - Anvisa Registration No. 80455630104
Kit Instrumental CMF Traumec Rev.04 - Anvisa Registration No. 80455630104
Kit Instrumental CMF Traumec Rev.05 - Anvisa Registration No. 80455630104
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