Scope: |
This ESSENTIAL describes the regulatory requirements for non-automated weighing instruments as defined in in Article 2 of 2014/31/AB(EU) for the following categories of instruments:
a) First category;
1) determination of mass for commercial transactions,
2) Bridge or road toll, tariff, tax, penalty, bonus, compensation or similar payments - determination of mass for calculation,
3) Application of relevant legislation provisions, determination of mass for expert opinion given in court minutes,
4) Determination of mass by weighing the patients for the purpose of medical monitoring, diagnosis and treatment,
5) Determination of mass for the preparation of the drugs in the prescription in the pharmacy and mass determination in the analyzes carried out in the medical and pharmaceutical laboratories,
6) For direct sales to consumers and pre-packaged products in public places of sale
b) The second category; determination of mass for all processes other than those listed in (a).
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Legislation in force: |
The applicable legislation is the Law No. 3516 of 1989.
Product Safety and Technical Regulations Law
The purpose of this Law is to ensure that the products are safe and comply with the relevant technical regulations; to determine the principles of market surveillance and inspection, the duties of authorized institutions and the obligations of economic operators and conformity assessment bodies.
The purpose of this Regulation is to determine the basic requirements for non-automatic weighing instruments and the procedures and principles regarding the conformity assessment procedures required for placing these instruments on the market.
It is the adoption of the Directive 2014/31/EU into the Turkish law.
CE Mark Regulation
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Comment on the comparability to EU legislation: |
The European Non-Automated Weighing Instruments Directive has been adopted in the form of Regulation 2014/31/AB:2016-07-02, plus harmonized standards.... |