Commission Decision of 16 December 2009 laying down guidelines for the management of the Community Rapid Information System ‘RAPEX’ established under Article 12 and of the notification procedure established under Article 11 of Directive 2001/95/EC (the General Product Safety Directive) (notified under document C(2009) 9843) (2010/15/EU) (repealed)
EU Decision 2010/15 · Adopted 16 December 2009 · Extends to United Kingdom
Commission Decision
of 16 December 2009
laying down guidelines for the management of the Community Rapid Information System ‘RAPEX’ established under Article 12 and of the notification procedure established under Article 11 of Directive 2001/95/EC (the General Product Safety Directive)
(notified under document C(2009) 9843)
(2010/15/EU) (repealed)
F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Annotations to the whole text
Textual amendments
Contents
- 1Article 1 Repealed
- 2Article 2 Repealed
- 3Article 3 Repealed
- Signature
- Annex: Guidelines for the management of the Community Rapid Information System ‘RAPEX’ established under Article 12 and of the notification procedure established under Article 11 of Directive 2001/95/EC (the General Product Safety Directive) Repealed
- Part I: STATUS AND ADDRESSEES OF THE GUIDELINES Repealed
- Status, objectives and updating of the Guidelines Repealed
- 1.1Status Repealed
- 1.2Objectives Repealed
- 1.3Updating Repealed
- 2Addressees of the Guidelines Repealed
- Part II: COMMUNITY RAPID INFORMATION SYSTEM ‘RAPEX’ ESTABLISHED UNDER ARTICLE 12 OF THE GENERAL PRODUCT SAFETY DIRECTIVE Repealed
- Introduction Repealed
- 1.1Objectives of RAPEX Repealed
- 1.2Components of RAPEX Repealed
- RAPEX notification criteria Repealed
- Division Repealed
- Consumer products Repealed
- 2.1.1Products covered by RAPEX Repealed
- 2.1.2Products which are not covered by RAPEX Repealed
- Measures Repealed
- 2.2.1Categories of measures Repealed
- 2.2.2Type of measures Repealed
- 2.2.3Obligatory measures initiated by authorities in charge of external border controls Repealed
- 2.2.4Exclusion of generally applicable obligatory measures Repealed
- 2.2.5Timing of the notification Repealed
- 2.2.6Notifying authorities Repealed
- 2.2.7RAPEX notification concerning business notifications Repealed
- Serious risk Repealed
- 2.3.1Serious risk Repealed
- 2.3.2Risk assessment method Repealed
- 2.3.3Assessing authority Repealed
- 2.3.4Risk assessment in business notifications Repealed
- Cross-border effects Repealed
- 2.4.1International event Repealed
- 2.4.2Local event Repealed
- Notifications Repealed
- Types of notifications Repealed
- 3.1.1RAPEX notifications Repealed
- 3.1.2Notifications for information Repealed
- Content of notifications Repealed
- 3.2.1Completeness of data Repealed
- 3.2.2Scope of data Repealed
- 3.2.3Updating of data Repealed
- 3.2.4Responsibility for the information transmitted Repealed
- Confidentiality Repealed
- 3.3.1Disclosure of information as a general rule Repealed
- 3.3.2Exceptions to the general rule Repealed
- 3.3.3Request for confidentiality Repealed
- 3.3.4Handling of notifications covered by confidentiality Repealed
- 3.3.5Withdrawal of request for confidentiality Repealed
- Examination of notifications by the Commission Repealed
- Division Repealed
- 3.4.1Correctness Repealed
- 3.4.2Completeness Repealed
- 3.4.3Requests for additional information Repealed
- 3.4.4Investigation Repealed
- Validation and distribution of notifications Repealed
- 3.5.1Validation and distribution of notifications Repealed
- 3.5.2Validation of notifications on safety aspects subject to discussions at EU level Repealed
- 3.6Information on dangerous products sent by the Commission Repealed
- Follow-up to notifications Repealed
- 3.7.1Follow-up to the different types of notification Repealed
- 3.7.2Objectives of the follow-up Repealed
- 3.7.3Follow-up techniques Repealed
- Permanent withdrawal of a notification from the RAPEX application Repealed
- Division Repealed
- 3.8.1Situations where withdrawal is possible Repealed
- 3.8.2Requesting Member State Repealed
- 3.8.3Content of the request Repealed
- 3.8.4Decision to withdraw Repealed
- Temporary removal of a RAPEX notification from the RAPEX website Repealed
- 3.9.1Situations where temporary removal is possible Repealed
- 3.9.2Requesting Member State Repealed
- 3.9.3Content of the request Repealed
- 3.9.4Decision to remove Repealed
- 3.9.5Re-publishing of a notification Repealed
- Deadlines for submitting RAPEX notifications Repealed
- 3.10.1Deadlines Repealed
- 3.10.2Emergency situations Repealed
- Reactions Repealed
- 4.1Communication of follow-up action Repealed
- Content of reactions Repealed
- 4.2.1Data provided Repealed
- 4.2.2Completeness of reactions Repealed
- 4.2.3Updating of validated reactions Repealed
- 4.2.4Responsibility for reactions Repealed
- 4.3Confidentiality Repealed
- Examination of reactions by the Commission Repealed
- 4.4.1Correctness and completeness Repealed
- 4.4.2Request for additional information Repealed
- 4.5Validation and distribution of reactions Repealed
- 4.6Permanent withdrawal of a reaction from the RAPEX application Repealed
- 4.7Deadlines for submitting reactions Repealed
- Operation of the RAPEX networks Repealed
- RAPEX Contact Points Repealed
- Division Repealed
- 5.1.1Organisation Repealed
- 5.1.2Tasks Repealed
- RAPEX networks established at EU and national levels Repealed
- 5.2.1RAPEX Contact Points Network Repealed
- 5.2.2RAPEX networks established at national level Repealed
- Means of communication, practical and technical arrangements for RAPEX Repealed
- 5.3.1Languages Repealed
- 5.3.2Online application for RAPEX Repealed
- 5.3.3Operation of RAPEX outside regular working hours Repealed
- Part III: NOTIFICATION PROCEDURE ESTABLISHED UNDER ARTICLE 11 OF THE GENERAL PRODUCT SAFETY DIRECTIVE Repealed
- 1Background and objectives Repealed
- 2Notification criteria Repealed
- 3Notifications Repealed
- 4Reactions Repealed
- 5Practical and technical arrangements Repealed
- Part IV: APPENDICES Repealed
- Standard notification form Repealed
- Reaction form Repealed
- 3Deadlines for Member States Repealed
- 4Deadlines for the Commission Repealed
- Risk Assessment Guidelines for Consumer Products Repealed
- 1Introduction Repealed
- Risk assessment – an overview Repealed
- 2.1Risk – Combination of hazard and probability Repealed
- 2.2A risk assessment in three steps Repealed
- Some useful tips Repealed
- Seek information Repealed
- Make a sensitivity analysis of your risk assessment Repealed
- Let others check your risk assessment Repealed
- Document your risk assessment Repealed
- Several hazards, several injuries – but only one risk Repealed
- Can risks cumulate? Repealed
- Compliance with limit values in legislation and standards Repealed
- Specific risk assessment guidelines in specific cases Repealed
- Building a risk assessment step by step Repealed
- Division Repealed
- 3.1The product Repealed
- The product hazard Repealed
- Division Repealed
- Hazard identification by tests and standards Repealed
- Products may still present a risk even though they do not cause injuries Repealed
- 3.3The consumer Repealed
- 3.4Injury scenario: Steps leading to injury(ies) Repealed
- 3.5Severity of injury Repealed
- 3.6Probability of injury Repealed
- 3.7Determination of risk Repealed
- 4From risk to action Repealed
- How to prepare a risk assessment – in brief Repealed
- 1Division 1 Repealed
- 2Division 2 Repealed
- 3Division 3 Repealed
- 4Division 4 Repealed
- 5Division 5 Repealed
- 6Division 6 Repealed
- 7Division 7 Repealed
- 8Division 8 Repealed
- 9Division 9 Repealed
- Examples Repealed
- 6.1Folding chair Repealed
- 6.2Socket protectors Repealed
- 6.3Sensitivity analysis Repealed