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In vitro diagnostics medical devices. Part 2. Automatic analyzer for immunoassays. Technical requirements for public procurement
Document status: Active
Medical electrical equipment. Mammographic stereotactic devices. Technical requirements for governmental purchases
Document status: Active
Medical devices. Biological evaluation of medical devices. Part 9. Framework for identification and quantification of potential degradation products
Document status: Replaced by GOST ISO 10993-9-2022
Guidelines for environmental auditing. Audit procedures. Auditing of environmental management systems
Document status: Cancelled
Medical electrical equipment. Part 2. Particular requirements for the safety of infant radiant warmers
Document status: Cancelled
Risk management of new technologies using. Part 2. Application to new technologies
Document status: Active