Regulatory ESSENTIAL
Europ. Economi. - NAWI Non Automatic Weighing Instruments

Scope of this ESSENTIAL

This ESSENTIAL describes the regulatory requirements for non-automated weighing instruments (NAWI) as defind in in Article 1 section for the following categories of instruments: (a) determination of mass for commercial transactions; (b) determination of mass for the calculation of a toll, tariff, tax, bonus, penalty, remuneration, indemnity or similar type of payment; (c) determination of mass for the application of laws or regulations or for an expert opinion given in court proceedings; (d) determination of mass in the practice of medicine for weighing patients for the purposes of monitoring, diagnosis and medical treatment; (e) determination of mass for making up medicines on prescription in a pharmacy and determination of mass in analyses carried out in medical and pharmaceutical laboratories; (f) determination of price on the basis of mass for the purposes of direct sales to the public and the making-up of prepackages; (g) all applications other than those listed in points (a) to (f). What is a "non-automated weighing instrument" (see 2.2 of the Directive): ‘non-automatic weighing instrument’ or ‘instrument’ means a weighing instrument requiring the intervention of an operator during weighing'

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 licence) 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)

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

Link/Reference to other reference document(s)

here you will get related hyperlink(s)

Link/Reference to other reference document(s)

here you will get a linked document in ROGER WILLCO (only reachable with additional ROGER WILLCO licence)

Link/Reference to other reference document(s)

here you will get related hyperlink(s)

Abbrevations

here you will get textual information 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

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

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.

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 related hyperlink(s)

Verification Regulation

here you will get related hyperlink(s) DE: Eichwesen

Hints

here you will get textual information Specific recommendations, information or most common mistakes

Regulatory labelling, markings and user information

Regulatory label (mandatory)

here you will get a image or chart e. g. product label

Regulatory label (mandatory)

here you will get a image or chart e. g. product label

Regulatory label (mandatory)

here you will get textual information 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

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

Code, Continent	EEA,
Economic Area
Official Language	24 official languages
Standard Institute
HS Codemember