Scope of this ESSENTIAL

This Essential describes the regulatory requirements as given by EU legislations (LVD and GPSR) for all laser products. Not included in this ESSENTIAL: Health of persons according to use of laser at the work place (see Directive 2006/25/EC) Medical devices with lasers (see Medical devices Directive 93/42/EEC and Medical devices Regulation (EU) 2017/745). '

Abbreviations

Here you will get a table Important abbreviations which are special for this legislation or theme.

Analysis of regulatory requirements

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)?

Scope of legislation

LVD: market access conditions for laser devices used for industrial and consumer purposes. Article 1: This Directive shall apply to electrical equipment designed for use with a voltage rating of between 50 and 1 000 V for alternating current and between 75 and 1 500 V for direct current, other than the equipment and phenomena listed in Annex II. Hint: If the voltage of the laser product is below the the voltage limits it is mandatory to use the GPSR.'

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)?

Responsible actors

Here you will get a linked document in ROGER WILLCO (only reachable with additional ROGER WILLCO license) 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

Link/Reference to other reference document(s)

Here you will get a linked document in ROGER WILLCO (only reachable with additional ROGER WILLCO license)

Market surveillance authority

Here you will get related hyperlink(s) Name of the authority for market surveillance and/or enforcement

Comment on the comparability to EU legislation

Here you will get textual information

Hints

Here you will get related hyperlink(s) Specific recommendations, information or most common mistakes

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]

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

Is the IECEE CB Scheme accepted by the authority/approval body?

Here you will get textual information "[Yes/ No / no information available] [Text] Information (website)"

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(s) to show compliance to the authority

Here you will get a linked document in ROGER WILLCO (only reachable with additional ROGER WILLCO license) 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 textual information 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 textual information

Source for standards for conformity assessment

Here you will get related hyperlink(s)

Are national standards based on IEC/ISO standards?

Here you will get textual information Undetailed information

Is in-country testing legally required?

Here you will get textual information

Acceptance of foreign test reports

Here you will get textual information

National Standardisation Organisation

Here you will get related hyperlink(s) Link to organisation

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 linked document in ROGER WILLCO (only reachable with additional ROGER WILLCO license) e. g. product label

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 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?

Warnings, symbols

Here you will get textual information e. g. ANSI Z 535.4

User instructions language(s)

Here you will get a table Regulated by the legal provisions

Hints

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

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