Regulatory ESSENTIAL



Regulatory ESSENTIALS - modular information package with all the essential information for compliant products in your target market. Conveniently read online at Product-Compliance-Portal ROGER WILLCO.

Scales; automatic weighing instruments; non automatic weighing instruments; Measuring Instruments; Type approval; Pattern approval; legal metrology, metrology mark; WELMEC; OIML; gravity zone; verification
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).

Stakeholders: Manufacturer, B2C products, B2B products
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

Application national: Turkey, Legal Metrology, Non-automated weighing instruments

Countries: Image for TR Turkey,  
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....
Status: Published 2020-05-04 by Anette Dunkel-Reinboth and Michael Loerzer
Last change 2024-04-10 by Anette Dunkel-Reinboth: Market surveillance authority, Metrology and legal metrology
ROGER WILLCO ID: #d86s
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Scope of this ESSENTIAL
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).'

Analysis of regulatory requirements

Measuring Device Type
Here you will get textual information

e. g. NAWI, AWI

Legislation in force for this PCT
Here you will get a linked document in ROGER WILLCO
(only reachable with additional ROGER WILLCO license)

Are legal provisions regulates the product compliance topic? If yes, what is the reference (title, number)?

Responsible actors
Here you will get textual information

Which actor(s) are responsible for compliance with the legal provisions: e. g. - economic operators (manufacturer, importer, distributor, fulfilment service provider), - user (commercial/industrial/professional), - user (private, consumer)?

Regulatory market access conditions for the actor(s)
Here you will get textual information

What are the main regulatory requirements (e. g. conformity assessment fulfilment of essential requirements of Annex I 2006/42/EC) prior placing on the market, importation and putting into service (brief description)

Penalty by this legislation
Here you will get textual information

What are the possible penalties (e. g. sales ban, fines) in the case of non-compliance?

Exemption clauses
Here you will get textual information

Exempted devices/products or industry sectors.

Sub-federal legislation of states/counties
Here you will get textual information

E. g. by 2019 an Inter-Governmental Agreement (IGA) on governance of the Electrical Equipment Safety System (EESS) has been signed by Queensland, Victoria, Western Australia and Tasmania.

FTA/MRA status with EU
Here you will get textual information

Has the country signed a Free Trade Agreement (FTA) or a Mutual recognition agreement (MRA) with EU?

Authority
Here you will get related hyperlink(s)

Name of the authority for approval, registration, market surveillance and/or enforcement

Market surveillance authority
Here you will get textual information

Name of the authority for market surveillance and/or enforcement

Comment on the comparability to EU legislation
Here you will get textual information

Abbrevations
Here you will get a table

Important abbreviations which are special for this legislation or theme.

Hints
Here you will get textual information

Specific recommendations, information or most common mistakes

Route to compliance

Formal and administrative requirements

Registration at related authority required?
Here you will get textual information

Product registration? Manufacturer registration? Importer / Representative registration? if required.

Local representative legally required?
Here you will get textual information

[Yes/No]

Member of International Metrology Organizations
Here you will get textual information

e.g. OIML

Hints
Here you will get textual information

Specific recommendations, information or most common mistakes

Equipment authorization (approval process)

Approval process (conformity assessment procedure)
Here you will get textual information

Means each legally required approval process prior placing on the market, importation or putting into service

Conformance document(s) to show compliance to the authority
Here you will get textual information

e. g. SDoC, technical documentation (for 10 years), filled-in approval forms (e. g. ACMA in AUT)

Conformance document validity and renewal
Here you will get textual information

Validity for Conformance document name mentioned. For mandatory certification validity is important.

Which documents are required by an approval body?
Here you will get textual information

e .g. formal application

Is a factory inspection legally required
Here you will get textual information

Hint to voluntary certification scheme
Here you will get textual information

If a important voluntary certification schemes exists, one link will be given. Important voluntary schemes are for example: UL, CSA, VCCI (Japan)

Testing & Standards

Specific requirements for testing
Here you will get textual information

e. g. is an accredited test lab. mandatory, limits, test samples, product description

General information to the application of standards
Here you will get textual information

e. g. China: GB standards are mandatory, EU: harmonized standards shall be published in the OJEU with respect to "presumption of conformity"

Source for standards for conformity assessment
Here you will get related hyperlink(s)

OIML Recommendations adopted?
Here you will get textual information

OIML is publishing international standards. IEC and ISO are not relevant for this theme.

National Standardisation Organisation
Here you will get related hyperlink(s)

Link to organisation

Is in-country testing legally required?
Here you will get textual information

Acceptance of foreign test reports
Here you will get textual information

Country gravity zones
Here you will get textual information

Verification Regulation
Here you will get textual information

DE: Eichwesen

Regulatory labelling, markings and user information

Regulatory label (mandatory)
Here you will get a image or chart

e. g. product label

Specific Metrology Marking(s)
Here you will get a image or chart

Regulatory e-labelling allowed?
Here you will get textual information

e. g. put the regulatory information and labels in a software menu

Required information on the product and/or packaging
Here you will get textual information

e. g. address of the manufacturer/importer, serial number

User instructions language(s)
Here you will get textual information

Regulated by the legal provisions

User instruction requirements and specific compliance notes
Here you will get textual information

Form, sentence inside, simple text. E. g. FCC/ISED compliance information, SAR information, battery, environmental information like waste

Digital user documentation allowed?
Here you will get textual information

User instructions allowed by QR-Code/internet or digital medium or integrated in device with display? Safety instruction allowed by QR-Code or digital medium?


Code, ContinentTUR, Europe/Asia
Economic AreaEUCU, BSEC (Black Sea Economic Cooperation)
Official LanguageTurkish - Law Numbered 805 on Mandatory Use of Turkish Language by Economic Enterprises | https://www.mevzuat.gov.tr/mevzuat?MevzuatNo=805&MevzuatTur=1&MevzuatTertip=3
Standard InstituteTSE Turkish Standards Instritute (Türk Standardları Enstitüsü) | https://www.tse.org.tr/en/
HS CodememberYes - since 1951






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