Alerta De Seguridad para all products manufactured by the company that manufactures medical-dental equipment, MZ INDÚSTRIA E COMÉRCIO LTDA

Brazilian data is current through June 2018. All of the data comes from Anvisa, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Brazil.

considering paragraph 3 of art. 111 of the Internal Regulation approved by Administrative Rule no. 593 of August 25, 2000, republished in the Official Gazette of December 22, 2000; considering the arts. 12 and 25 of Law no. 6,360, September 23, 1976; considering items XXIX, XXXV of art. 10, of Law no. No. 6,437, August 20, 1977; considering items IX, X, XV, XXIV, all of art. 7 of Law No. 9,782, of January 26, 1999; considering CVS communiqué 350/2003 GT Correlatos DITEP, published in the Official Gazette of the State of São Paulo on October 16, 2003, regarding the Notice of Infringement No. 01015 ¿AIP 01059 and TIP 02464, drawn up by the Municipal Health Department of Ribeirão Black, on the 25th day of February 2003