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Laws and Rules
RDC 15/2012 - ANVISA - Requirements and Good Practices for the Processing of Health Products
RDC 185/2001 - ANVISA - Registration and Exemption of Related Products
RDC 51/2009 - ANVISA - Efficiency of Disinfectants/Sterilizers against Mycobacterium Massiliense
General Guidance Manual for CME by ANVISA
RDC 55/2012 - Enzymatic Detergents for Restricted Use in Health Care Establishments
RDC 2606/2006 - Guidelines for the Development, Validation and Implementation of Medical Device Reprocessing Protocols
RDC 2605/2006 - Indication of products that at the current stage of knowledge should not be reprocessed
RDC 50/2002 - Reg. Tech p Planning, prog. , elab. , and endorsement. of physical establishment projects. health care
RDC 06/2013 - Requirements for Good Operating Practices for serv. endoscopy with access to the body through exclusively natural orifices
RDC 02/2010 - Management of Health Technologies in Health Facilities
RDC 08/2009 - Measures to Reduce Ocor. of Rapidly Growing Mycobacterial Infections - RCM in Health Services
Joint Risk Notice 001/2013 - Use of Crochet Needles as a Surgical Instrument in Peripheral Vascular Surgery Procedure
RDC 156/2006 - Registration, Labeling and Reprocessing of Medical Products
CVS 264/2008 - Prohibition of the Use of the Improper Device "Domestic" Drills without ANVISA Registration in Surgical Procedures
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