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  • Electrical equipment prohibited from the market

The Belgian Official Journal of 9 March 2004 published two lists of electrical equipment prohibited from the market. One concerns 111 devices not complying with the "Low voltage" Directive - LVD: 73/23/EEC. The other concerns 27 products not complying with the EMC Directive - 89/336/EEC.

All products were already prohibited in another EEA Member State.

Click here to access the LVD list (Dutch and French only);
Click here to access the EMC list (Dutch and French only).

Our page on "Forbidden & dangerous devices on the market" gives a permanent link to such lists.

 9/3/2004 Top of Page


  • Re-writing the low voltage Directive

On 6 February 2004, the European Commission issued the version 5 of the draft revision of the "Low Voltage Directive" (LVD) - 73/23/EEC.

That version has still some open wording. Nevertheless, it will be submitted in 2004 to an extended impact analysis to determine the economical social and environmental effect of the proposed changes. Indeed, the latter are rather fundamental. If a good deal of those is only a wording more in line with the current wording of "New approach" directives, some new concepts were introduced:

  • No lower limit in voltage: all devices are covered from 0 Volt upward;
  • A risk analysis must be performed for all electrical equipment concerned. However, applying the relevant harmonised standards will satisfy this requirement;
  • "Benign electrical equipment" is defined as those for which the risk analysis has shown that they present negligible hazards. A "Simple conformity assessment procedure" is defined for them;
  • Extended list of hazards and requirements to be considered, including the principles of safety integration, incorrect functioning, various fields, and ergonomics;
  • Extended labelling and instruction for the installers and users.

Click here to read the full text of the draft - Version 5 (English only).

 8/3/2004 Top of Page


  • Weekly updates of the RAPEX publicly available

The General Product Safety Directive - GPSD - (2001/95/EC) has established the legal basis for the Rapid Alert System for Non-Food Products - RAPEX.

Click here to access our latest news on the GPSD.

The RAPEX concerns dangerous consumer products. It is used by the EEA members to rapidly exchange information on such products. Now, the European Commission makes that information publicly available on its website. Updates are usually done on a weekly basis. Two to four products are generally added by every update to the system.

Click here to access the RAPEX website (English only).

We permanently link with the RAPEX website from our page on Forbidden & Dangerous Devices.

 3/3/2004 Top of Page


  • Managing the risks of active implantable medical devices

The Official Journal of the European Union of 18 February 2004 publishes the reference to the standard EN ISO 14971:2000/AC:2002 Medical devices - Application of risk management to medical devices in the framework of the Directive 90/385/EEC on active implantable medical devices. That standard is since then considered as "harmonised" and therefore confers a presumption of conformity to the directive when used for the design and production of such devices.

The reference of that standard was previously published on 31 July 2002 in the framework of directives 93/42/EEC concerning medical devices and 98/79/EC on in vitro diagnostic medical devices.

Read the corresponding communication in: English, français, Nederlands

 27/2/2004 Top of Page


  • Revision of the European directive on packaging

The Official Journal of the European Union of 18 February 2004 publishes the Directive 2004/12/EC of the European Parliament and of the Council of 11 February 2004 amending Directive 94/62/EC on packaging and packaging waste.

This revision completes the definition of packaging by introducing three new criteria. Examples are supplied as Annex I to the Directive.

It also re-defines the obligations of the Member States regarding prevention, and recovery and recycling of packaging waste. Further, it introduces a revision process to be repeated every five years.

This Directive must be transposed into the national legislations by 18 August 2005.

Read the full text of the Directive in: English, français, Nederlands

 26/2/2004 Top of Page


  • Amendments of the Belgian General Regulation on Electrical Installations - AREI/RGIE

Since September 2003 we announce the coming publication of amendments of the Belgian General Regulation on Electrical Installations - AREI/RGIE. That publication has started. Four Royal Decrees have already been published in the Belgian official journal of 17, 18, 24 and 26 February 2004.

Read the full text of the decrees (Dutch and French only):

Articles Object Click
28, 79, 80, 81, 82, 88, 94, 199, and 240 Terminology related to the earthing.

Here

57 Procedures of cutting, welding and associated procedures using an electric arc.

Here

98 and 99 Prevention of electric shocks by indirect contact at high voltage.
Prevention of electric shocks by indirect contact following propagation of potential.
Here
(540 kB)
242 Discharge lamps which are not part of public lighting installations and which are supplied by a transformer, converter or inverter with a no-load rated output voltage greater than 1 kV but not exceeding 10 kV. Here

Seven Royal Decrees amending 54 other articles are still expected. To access the draft decrees, read our news of:

24/9/2003
2/10/2003
23/10/2003

 26/2/2004 Top of Page


  • Clean hot-water boilers for Belgium

The Belgian Official Journal of 30 January 2004 has published the Royal Decree of 8 January 2004 regulating the levels of nitrous oxide (NOX) and carbon mono-oxide (CO) emissions for central-heating boilers and burners fed with liquid or gaseous fuel with a rated output of no more than 400 kW.

The decree specifies the maximum level of emissions for different types of equipment and fuels. Before putting a new equipment on the market, the manufacturer or its representative in the European Union submits that equipment to a type-evaluation by a recognised body and establishes a declaration of conformity (in Dutch, French and German) to the maximum emission levels specified for its equipment. The production is followed-up by a recognised body either by unannounced inspection visits or by monitoring of its quality system (ISO 9001).

The decree will be applicable on 31 January 2005. 

Click here to read the Royal Decree (Dutch and French only).

 10/2/2004 Top of Page


  • A new list of harmonised standards for ATEX

The Official Journal of the European Union of 24 January 2004 publishes the latest list of harmonised standards related to the Directive 94/9/EC (ATEX).

It is good to know that products complying with the requirements of an harmonised standard are presumed to comply with the corresponding requirements of the Directive.

Read the full list of standards in: English, français, nederlands

 27/1/2004 Top of Page


  • Products and services safety: upgrading the guidance

The Belgian transposition of the Directive 2001/95/EC has been previously discussed. (Click here to read the related news.) On 19 January 2004, the Product Safety Service of the Belgian authorities has issued a revision of its former guidance document.

Besides some details added in certain areas, the new document gives now a road map to bring a safe product on the market.

Read the full text of the guidance in: français, nederlands

 27/1/2004 Top of Page


  • Two years guarantee for consumer goods in Belgium?

The Directive 1999/44/EC of the European Parliament and of the Council of 25 May 1999 on certain aspects of the sale of consumer goods and associated guarantees prescribes that all consumer goods are guaranteed for a period of two years as from its delivery. This applies to both new and second-hand goods. For the latter, the Member States may allow that the supplier limits its guarantee in time but to not less than one year.

This Directive had to be transposed in national legislations of all EU Member States by 1 January 2002.

On 23 July 2003, Belgium was condemned by the European Court of Justice for failing to transpose the Directive. It is still not done. What are the consequences for the manufacturers supplying consumer goods in Belgium and in the other EU member States and for the Belgian consumers?

Suppliers of consumer goods must obey the law applicable where they sell products. Therefore, manufacturers must offer a two years guarantee for the consumer goods they supply in EU but outside of Belgium. In Belgium, they may still limit their guarantee to one year for new products and to nothing for second-hand goods.

Today, it remains difficult for the Belgian consumer to benefit from the Directive. Of course, if he buys a good abroad in EU, the two years guarantee will apply but with the burden to refer to foreign law and supplier services. If he buys the good in Belgium and if he is refused a guarantee of two years, he can act in court against Belgium that is liable for not complying with its obligations within the EU treaties. He will most probably win his case but when? and after which efforts?

Read the full text of the Directive in: English, français, nederlands
Read the full text of the judgement in: English, français, nederlands

 19/1/2004 Top of Page


  • Acoustical noise from household appliances

The Official Journal of the European Union of 16 January 2004 published the revised list of harmonised standards under the Council Directive 86/594/EEC of 1 December 1986 on airborne noise emitted by household appliances.

Read the list of standards in: English, français, nederlands

 19/1/2004 Top of Page


  • Financing the management of historical WEEE's

The Official Journal of the European Union of 31 December 2003 published the Directive 2003/108/EC of the European Parliament and of the Council of 8 December 2003 amending Directive 2002/96/EC on waste electrical and electronic equipment (WEEE).

This amendment details how to finance the management of historical WEEE from users other than private household. The initial provisions of the Directive 2002/96/EC raised questions from the industry. Now, the financing depends on replacement or not of the related equipment. If the WEEE is replaced, the supplier of the new equipment takes care of the WEEE. However, the Member States may stipulate that the user also be made, partly or totally, responsible for the financing. If there is no replacement, the financing is always provided by the user.

Read the full text of the Directive in: English, français, nederlands

 15/1/2004 Top of Page


  • Assuring the safety of products and services

The European Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety - GPSD - becomes strictly applicable on 15 January 2004 in the EEA territory. It supersedes the initial directive of 1992.

The new Directive has a broader scope as it encompasses not only the consumer products but all services rendered to consumers with such products. A peculiarity is that this directive must be read in conjunction with any directive covering a specific product. When such a directive exists, the GPSD ceases to apply for the aspects covered by the specific directive. This means that it still applies for what is not treated in the specific directives.

This leads to an embarrassing question: What should be retained from the GPSD in a particular case?

To help finding the appropriate answer, the EC (DG SANCO) has issued a guidance document analysing the relation between the GPSD and the Toys Directive (88/378/EEC), the low voltage directive (LVD: 73/23/EEC), the directive on personal protective equipment (PPE: 96/58/EC) and the cosmetics directive (76/768/EEC). There is however no guarantee that this analysis is correct. Only the European Court of Justice may interpret the Community law.

Click here to read the guidance document (English only)

Considering that source and without any guarantee, our opinion regarding directives in our activity area is as follows:

  • LVD
    • All possible risks are covered by the LVD.
    • The GPSD provides a legal basis for current administrative practices.
    • For the professionals, the main implications of the GPSD are:
      • Identification of the products to assure traceability.
      • Market monitoring and action when a problem with the product is detected.
      • Obligation to inform the authorities of problems occurring and obligation to co-operate with them to prevent risks.
      • Similar obligation for the distributors.

       

  • EMC (89/336/EEC)

    The EMC directive covering a risk and no specific products, the GPSD should not interfere.

     

  • Medical Devices (MDD: 93/42/EEC)
    • All possible risks are covered by the MDD.
    • The administrative provisions being extensively developed within the MDD, the GPSD should not have a significant impact.

In Belgium, the GPSD has been transposed by the law of 9/2/1994 amended for the last time by the law of 18/12/2002. That transposition has a much broader scope than the GPSD. Indeed, not only it covers the consumer products and services but also products and related services of the professional sphere. All products and services are concerned.

Beside the fact that the scope is broader, the provisions of the Belgian law are those of the GPSD. To clarify the application of the law in the Belgian context, the authorities have issued a Q&R document. Once again, that document is not legally binding but represents the views of the authorities in that matter.

Read the Belgian Q&R document in: français, nederlands

 13/1/2004 Top of Page


  • Harmonised standards for the EMC

The Official Journal of the European Union of 12 November 2003 published an updated list of harmonised standards relating to electromagnetic compatibility - EMC.

It should be noted that many standards have been recently replaced, the superseded standards loosing their applicability in 2004.

Access the list of EMC standards in: English, français, nederlands

 9/1/2004 Top of Page


  • New standards for the medical devices

The Official Journal of the European Union of 11 November 2003 published three new harmonised standards relating to medical devices. These standards cover the biological evaluation and the clinical investigation of medical devices, two crucial areas.

Clinical data are always requested to demonstrate the compliance of a medical device with the regulation. Furthermore, clinical investigations are requested for Class III devices and for implantable and long-term invasive devices falling within Class IIa or IIb. 

Access the list of new standards in: English, français, nederlands

 9/1/2004 Top of Page


  • The "Cassis de Dijon" case strikes again!

On 4 November 2003, the Official Journal of the European Union published the Commission interpretative communication on facilitating the access of products to the markets of other Member States: the practical application of mutual recognition (2003/C 265/02).

The principle of mutual recognition in the area of intra-Community transfers of products is stated in articles 28 and 30 of the EC Treaty. But what does it mean in practice? Of course, free movement is guaranteed to products dully bearing the CE marking but what about those other products that are allowed in a given country? Could they be freely exported to another European country?

Since the ruling of the European Court of Justice in the "Cassis de Dijon" Judgment of 20 February 1979, it is clear that, in principle, a product which is legally marketed in a given Member State of the European Economic Area (EEA) or in Turkey can be marketed in any other country provided it provides an equivalent level of protection of the various legitimate interests at stake.

Is this really clear? The communication of the Commission explains in details what it means and how the principle of mutual recognition should be applied.

Read the full text of the communication in: English, français, nederlands

 15/12/2003 Top of Page


  • ET evaluates security firms

 

Electro-Test - ET, our partner for the INCERT certification of installers of alarm systems, has been recognised by M Patrick DEWAEL, Belgian Minister of Interior, for the evaluation of security companies wishing to be recognised in the framework of the law of 10 April 1990.

According to the law, security firms are firms offering to third parties services of design, installation, maintenance, or repair of alarm systems. Such firms must be evaluated and monitored by inspection bodies recognised by the Minister of Interior, such as Electro-Test. In that function, ET verifies that the security firms comply with the requirements of the Royal Decree of 13 June 2002 on the recognition of security firms. The latter include compliance with the Technical note T015/2 (General requirements for the certification of security companies and of installers of alarm systems) issued by the Belgian Electrotechnical Committee (BEC). This note is also the basis for the INCERT certification of security firms.

Click here for more details on INCERT.

Click here to read the notification of the Minister of Interior (Dutch and/or French).

 12/12/2003 Top of Page


  • Putting cable reels on fire

 

The 9 December 2003 issue of the Official Journal of the European Union publishes the Commission opinion of 8 December 2003 within the framework of Council Directive 73/23/EEC relating to electrical equipment designed for use within certain voltage limits - Safety of cable reels.

The Swedish authorities have noticed that electrical cable reels complying with the EN 61242 standard could be set on fire when subject to a maximum load and when the cable is not completely unrolled. In such a case, the insulation material can melt and live parts may be accessible. This is of course an intolerable risk and a non-compliance with the essential requirements of the Directive.

After review of the problem, the EC concluded that:

  • The EN 61242 is not regarded as giving a presumption of conformity with regard to the risk of fire and electrical shock in cases of foreseeable overload;
  • Manufacturers may use thermal or current cut-outs or other appropriate means to cover these risks;
  • Member States should consider those risks in their market surveillance activities.

We should also advise the owners of cable reels to examine whether the latter are protected against overheating. If not, they should always be used completely unrolled or replaced.

Read the full text of the Commission opinion in: English, français, nederlands

 10/12/2003 Top of Page


  • Protecting workers against electromagnetic fields - EMF

 

On 20 October 2003, the European Commission announced that an agreement has been found on a new Directive on the protection of workers against electromagnetic fields.

The Directive targets hazards generated by power generation installations, broadcasting antennae, mobile phone antennae, radar installations, large furnaces and other industrial installations. It also addresses risks incurred by workers exposed during long periods to devices such as anti-theft gates used in shops.

The Directive concerns electromagnetic fields in the range of 0 Hz to 300 GHz. It addresses the risk to the health and safety of workers due to known short-term adverse effects in the human body. It does not address suggested long-term effects. The text fixes limits to be observed to ensure protection against adverse effects.

Read the full text of the proposed Directive in: English, nederlands

It should be noted that the protection of the population has been dealt with by the European Council on 12 July 1999 in a Recommendation.

Read the full text of the Recommendation in: English, français, nederlands

Most of the scientific work done in that area is carried out in the framework of the International Commission on Non-Ionizing Radiation Protection - ICNIRP. Click here to visit their website.

 23/10/2003 Top of Page


  • More more draft amendments of the Belgian General Regulation on Electrical Installations - RGIE/AREI

 

The Official Journal of the European Union of 22 October 2003 references a new draft Royal Decree amending 8 articles of the Belgian General Regulation on Electrical Installations - RGIE/AREI.

The standstill period during which the draft may not be adopted extends till 2 January 2004. Comments or questions can be sent directly to the Belgian authorities at: belnotif@mineco.fgov.be

The draft concerns measures to prevent fire in electrical installations and to improve the behaviour of such installations during fire. It also introduces the notion of "vital consumer" and of "vital circuits". During fires, such circuits must remain operational during at least 1 hour. For high rise buildings and buildings accessible to the public, the material of the cables must not produce toxic or opaque smokes when on fire.

Read the full text of the draft in: English, français, nederlands

 23/10/2003 Top of Page


  • Updating the list of harmonised standards for the EMC Directive

 

The Official Journal of the European Union of 22 July 2003 published an updated list of the harmonised standards giving a presumption of conformity to the requirements of the EMC Directive (89/336/EC - Electromagnetic compatibility).

It should be noted that the limit of validity of the superseded standard EN 55022:1994 "Limits and methods of measurement of radio disturbance characteristics of information technology equipment" has been postponed till 1st August 2005 whilst the "new" EN 55022:1998 is already applicable. This gives some more time to get acquainted with the technical solutions needed to apply the new standard.

Click here to access the dedicated webpage on the Europa website.

 13/10/2003 Top of Page


  • More draft amendments of the Belgian General Regulation on Electrical Installations - RGIE/AREI

 

The Official Journal of the European Union of 1st October 2003 references six draft Royal Decrees amending 40 articles of the Belgian General Regulation on Electrical Installations - RGIE/AREI.

The standstill period during which the drafts may not be adopted extends till mid-December. Comments or questions can be sent directly to the Belgian authorities at: belnotif@mineco.fgov.be

Click to read the drafts in:

Draft Object EN FR NL
Art. 3, 22 to 27, 32, 40, 86, 88, 202, 203, 220 and 221 Introduction of the notion of very low voltage. New rules for bathrooms. Here Ici Hier
Art. 90, 91 and 92 New rules for swimming pools, saunas, fountains and other water pools. Use of very low voltages. Here Ici Hier
Art. 242 New rules for the installation of discharge lamps. New protections against earth leakage and open circuits. Here Ici Hier
Art. 15, 18, 66, 76, 77, 80, 94, 120, 169, 175, 181, 190, 199, 207, 236, 239, 240 and 260 Various linguistic corrections.
IPXX-B minimum for plugs.
New rules for high power connectors.
NA Ici Hier
Art. 74 and 251 Conformity with HD 637.
Various prescriptions for high voltage installations.
NA Ici Hier
Art. 29, 86, 207 and 227 Precisions regarding the IP code, earthing cables and thermoplastic conduits. NA Ici Hier
 2/10/2003 Top of Page


  • Draft amendments of the Belgian General Regulation on Electrical Installations - RGIE/AREI

 

The Official Journal of the European Union of 24 September 2003 references three draft Royal Decrees amending 15 articles of the Belgian General Regulation on Electrical Installations - RGIE/AREI.

Two drafts concern the prevention of electric shocks by indirect contact at high voltage or due to the propagation of the potential. The third draft relates to the codification of people and to the conditions of work in the vicinity of electrical installations.

Click to read the drafts in:

Draft EN FR NL
Art. 28, 79, 80, 81, 82, 88, 94, 199 and 240 Here Ici Hier
Art. 98 and 99 Here Ici Hier
Art. 47, 192, 196 and 266 Here Ici Hier
 24/9/2003 Top of Page


  • CEBEC notified for the Medical Devices Directive

 

On 16 July 2003, the Belgian Minister of Public Health, Mr. Rudy Demotte, confirmed that he will notify CEBEC to the European Commission as a body recognised for performing the assessment procedures foreseen by the art. 5 of the Royal Decree of 18 March 1999 transposing the Directive 93/42/EEC on medical devices.

This notification concerns the annexes II (full quality assurance system), III (EC type-examination), IV (EC verification), V (production quality assurance) and VI (product quality assurance). It covers:

  • Active medical devices but those emitting ionising radiations and those designed to image in-vivo the dispersion of radiopharmaceutical products
  • Non invasive devices limited to those designed :
  • to immobilise or to apply a force or pressure on the body or parts of the body
  • to stand patient bodies (beds...)
  • for miscellaneous uses (stethoscopes, non invasive electrodes...)
  • Re-usable surgical instruments

It also concerns the verification of mechanical, electrical and electromechanical aspects of medical devices of classes I, IIa and IIb using ionising radiations according to the annexes III and IV but for the nuclear aspects.

Click here to read the full text of Minister Rudy Demotte letter (French only).

 8/9/2003 Top of Page



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