We are migrating the content of this website during the first semester of 2014 into the new EUR-Lex web-portal. We apologise if some content is out of date before the migration. We will publish all updates and corrections in the new version of the portal.
Do you have any questions? Contact us.
Non-automatic weighing instruments
The Commission highlights the necessity for harmonised European standards in the field of metrology to protect the public against incorrect results of weighing operations. This Directive therefore defines the requirements for non-automatic weighing instruments.
Directive 2009/23/EC of the European Parliament and of the Council of 23 April 2009 on non-automatic weighing instruments (Codified version) (Text with EEA relevance).
This Directive aims at harmonising the rules which apply to non-automatic * weighing instruments * in order to ensure their free movement in the internal market and to protect the public against the consequences of incorrect weighing results.
This Directive covers weighing instruments used for:
- commercial transactions;
- the calculation of a toll, tariff, tax, bonus, penalty, remuneration, indemnity or similar type of payment;
- the application of laws or regulations, or for an expert opinion given in court proceedings;
- the practice of medicine, in particular for weighing patients for the purposes of monitoring, diagnosis and medical treatment;
- making up medicines on prescription in a pharmacy and in analyses carried out in medical and pharmaceutical laboratories;
- the determination of price on the basis of mass for the purposes of direct sales to the public and the making-up of pre-packages;
- any other application.
Placing on the market
The Member States are to ensure that only instruments complying with the essential requirements set out in Annex I of the Directive and bearing the “CE” marking are placed on the market. They may only block their placing on the market if they consider that these instruments do not meet the requirements of the Directive. In this case, they may prohibit or restrict their being placed on the market. They must inform the Commission thereof and give the reasons justifying their decision.
Manufacturers may choose between two conformity assessment methods to obtain the certificate of conformity for their products:
- EC type examination followed by either the EC declaration of type conformity or EC verification;
- EC unit verification.
Member States shall notify the Commission, as well as other Member States, of the bodies which they have appointed to carry out conformity assessment procedures, the specific tasks assigned to these bodies, and their identification numbers.
“CE” conformity marking and inscriptions
“CE” conformity marking should be affixed in a visible and indelible form on instruments for which CE conformity has been established. Any other marking may be affixed provided that it does not hinder understanding by third parties of the signification of CE marking and that it does not reduce its visibility or legibility.
Directive 2009/23/EC repeals Directive 90/384/EEC.
|Act||Entry into force||Deadline for transposition in the Member States||Official Journal|
OJ L122 of 16.5.2009