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 (NAWI) acc. to Ordinance of the FDJP on non-automatic weighing instruments NSWV (law 941.213) as defined in Article 2 (Scope) and the legal obligations for manufacturers (Annex 6) Article 2: Non-automatic weighing instruments are subject to this regulation if they are used for: a) Determination of the mass in trade and business, as well as with regard to the preparation of expert opinions for judicial purposes and the application of legal provisions, in particular for the calculation of a fee, duty, levy, allowance, penalty, remuneration, compensation or similar payments; b) determination of the mass when weighing patients in the context of medical monitoring, examination and treatment, in the manufacture of medicinal products in pharmacies on the basis of a doctor's prescription and in analyzes in medical and pharmaceutical laboratories; c) Determination of the price according to the mass for sales in open sales outlets and for the manufacture of prepackages.

Stakeholders: Manufacturer, B2C products, B2B products
Legislation in force: Federal Law of Metrology (SR 941.20) - (MessG) in force since 1 January 2013 Content: Chapter 1: General provisions Chapter 2: Placing measuring equipment on the market Chapter 3: Subsequent control Chapter 4: Measures Chapter 5: Information Chapter 6: Implementation and final provisions Appendix 1: Initial requirements for the measuring equipment Appendix 2: Conformity assessment of measuring equipment Appendix 3: Obligations of economic operators Appendix 4: Conformity Marks Appendix 5: Approval procedure and initial calibration Appendix 6: List of characters Appendix 7: Procedures for maintaining measurement stability Ordinance of the FDJP/EJPD on non-automatic weighing instruments - NSWV (SR 941.213) in force since 1 May 2004 Instruction on the Ordinance of the FDJP on non-automatic weighing instruments, in force since 1 July 2019 Content: a) to determine the mass in trade and business, i.e. goods that are bought or sold by weight, including B2B transactions and to determine the weight of goods in open sales in accordance with Article 5 of the Quantity Information Ordinance from September 5, 2012 (MeAV; SR 941.204); b) for the application of legislation, such as the calculation of a fee, duty, tax or similar, e.g. scales to determine waste charges; c) for the commercial determination of transport or service fees, e.g. letter and parcel scales, scales for luggage in airports and train stations, scales in laundries; d) to prepare expert reports for judicial purposes, provided the scales are not used by persons who are experts in the field of measurement technology; e) for the monitoring of traffic by the police, e.g. axle load scales; f) for weighing patients as part of medical treatment by authorized medical personnel, e.g. bathroom scales in hospitals or health centers; g) for the production of medicines in pharmacies based on medical prescriptions; h) for analyzes in medical and pharmaceutical laboratories that carry out analyzes on behalf of a doctor; i) in open sales outlets that display or print the price of the goods; j) for the weighing and labeling of prepackages of unequal nominal quantities (random packs; Art. 27 MeAV), so-called price labeling scales; k) to check the filling quantity of prepackages (Art. 33 Para. 2 MeAV); l) for the counting of ballot papers; m) to determine the number of items by weight, so-called counting scales.

Application national: Switzerland, Legal Metrology, Non-automatic weighing instruments,

Countries: Image for CH Switzerland,  
Comment on the comparability to EU legislation: Almost similar to EU legislation....
Status: Published 2020-05-11 by Anette Dunkel-Reinboth and Michael Loerzer
Last change 2024-03-04 by Torsten Sahm: Abbrevations, Metrology and legal metrology
ROGER WILLCO ID: #c86z
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Scope of this ESSENTIAL
This ESSENTIAL describes the regulatory requirements for non-automated weighing instruments (NAWI) acc. to Ordinance of the FDJP on non-automatic weighing instruments NSWV (law 941.213) as defined in Article 2 (Scope) and the legal obligations for manufacturers (Annex 6)

Article 2:
Non-automatic weighing instruments are subject to this regulation if they are used for:
a) Determination of the mass in trade and business, as well as with regard to the preparation of expert opinions for judicial purposes and the application of legal provisions, in particular for the calculation of a fee, duty, levy, allowance, penalty, remuneration, compensation or similar payments;
b) determination of the mass when weighing patients in the context of medical monitoring, examination and treatment, in the manufacture of medicinal products in pharmacies on the basis of a doctor's prescription and in analyzes in medical and pharmaceutical laboratories;
c) Determination of the price according to the mass for sales in open sales outlets and for the manufacture of prepackages.'

Abbrevations
Here you will get textual information

Important abbreviations which are special for this legislation or theme.

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)?

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)

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 related hyperlink(s)

Name of the authority for market surveillance and/or enforcement

Link/Reference to other reference document(s)
Here you will get a linked document in ROGER WILLCO
(only reachable with additional ROGER WILLCO license)

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

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)

Hints
Here you will get related hyperlink(s)

Specific recommendations, information or most common mistakes

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)

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

Link to organisation

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 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

Hints
Here you will get textual information

Specific recommendations, information or most common mistakes


Code, ContinentCHE, Europe
Economic AreaEFTA
Official LanguageGerman, French, Italian, Romansh - Sprachengesetz, SpG |https://www.fedlex.admin.ch/eli/fga/2006/1176/de
Standard InstituteSchweizerische Normen-Vereinigung (Swiss Association for Standardization) - SNV |https://www.snv.ch/de/
HS CodememberYes






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