M/433 - Graphical symbols
Standardisation mandate addressed to CEN and CENELEC within the framework of Directive 2007/47/EC, amending Directive 93/42/EEC relating to Medical Devices, concerning graphical symbols for use in the labelling of medical devices containing phthalates
General Information
Frequently Asked Questions
A European Standardization Mandate is a formal request from the European Commission to the European Standardization Organizations (CEN, CENELEC, and ETSI) to develop European standards (ENs) in support of EU legislation and policies. Mandates are issued under Regulation (EU) No 1025/2012 and help ensure that products and services meet the essential requirements set out in EU directives and regulations.
M/433 is a European Standardization Mandate titled "Standardisation mandate addressed to CEN and CENELEC within the framework of Directive 2007/47/EC, amending Directive 93/42/EEC relating to Medical Devices, concerning graphical symbols for use in the labelling of medical devices containing phthalates". Standardisation mandate addressed to CEN and CENELEC within the framework of Directive 2007/47/EC, amending Directive 93/42/EEC relating to Medical Devices, concerning graphical symbols for use in the labelling of medical devices containing phthalates There are 2 standards developed under this mandate.
Standards developed in response to a mandate and cited in the Official Journal of the European Union become "harmonized standards". Products manufactured in compliance with harmonized standards benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation, facilitating CE marking and market access across the European Economic Area.
This European Standard specifies requirements for the labelling of a medical device or parts of a medical device to indicate the presence of phthalates, when required by Annex I of Directive 93/42/EEC Section 7.5, 2nd paragraph. This specifically includes the format of a symbol to be used in the labelling. This European Standard does not specify the requirements for information to be supplied with medical devices, which are addressed by EN 980 and EN 1041.
This European Standard does not specify the requirements of the 1st and of the 3rd paragraphs of Essential Requirement 7.5.
- Standard12 pagesEnglish languagee-Library read for1 day
This European Standard specifies requirements for the labelling of a medical device or parts of a medical device to indicate the presence of phthalates, when required by Annex I of Directive 93/42/EEC Section 7.5, 2nd paragraph. This specifically includes the format of a symbol to be used in the labelling. This European Standard does not specify the requirements for information to be supplied with medical devices, which are addressed by EN 980 and EN 1041.
This European Standard does not specify the requirements of the 1st and of the 3rd paragraphs of Essential Requirement 7.5.
- Standard12 pagesEnglish languagee-Library read for1 day