Article eec number sheet dimensions

OJ L Avis juridique important. Whereas it is important to adopt measures with the aim of progressively establishing the internal market over a period expiring on 31 December ; whereas the internal market shall comprise an area without internal frontiers in which the free movement of goods, persons, services and capital is ensured.

article eec number sheet dimensions

Whereas rules on certain dangerous preparations having very specific uses have already been laid down:. Whereas, despite the abovementioned Community provisions, the rules, if any, applying to certain dangerous preparations in the Member States exhibit considerable differences as regards classification according to the degree of risk; whereas these differences constitute a not insignificant barrier to trade and directly affect the establishment and functioning of the common market.

Whereas this Directive must, at the same time, ensure protection for the general public and, in particular, of persons who come into contact with dangerous preparations in the course of their work or in the pursuit of a hobby, of consumers, especially children and the visually handicapped, and also for the environment. Whereas the label constitutes a basic tool for users of the preparations by giving them the initial essential concise information; whereas it nevertheless needs to be supplemented by a two-fold system of more detailed information, one intended for professional users, and the second for the bodies appointed by the Member States and whose responsibility it is to give information reserved solely for medical purposes, both curative and preventive.

Whereas dangerous preparations may, although conforming to the provisions of this Directive, nevertheless constitute a danger to health or the environment; whereas it is therefore advisable to provide a procedure to reduce this danger. Article 1 1. The purpose of this Directive is to approximate the laws, regulations and administrative provisions of the Member States on the:.

This Directive shall apply to preparations which are placed on the market in the Member States and which:. Article 3 1. The health hazards of a preparation shall be assessed by one or more of the following methods:. Any one or more of the toxicological properties of the preparation which are not assessed by the method set out in b hereof shall be assessed in accordance with the conventional method. Where a toxicological property has been established by both the methods above, the result of method b shall be used for classifying the preparation except in the case of carcinogenic, mutagenic and teratogenic effects.

For preparations of a known composition classified in accordance with method 3 b above a new health hazard assessment either by method 3 a or b shall be performed whenever:. In accordance with Article 3 3 athe health hazards shall be assessed by the conventional method described below, using individual concentration limits.

However, this substance must be treated on the same basis as the other substances present in the preparation when applying the method of evaluation by calculation, if the labelling gave at least an indication of the health hazard. LXn is the limit specified for each very toxic, toxic or harmful substance expressed as a percentage.

LC, R 35 is the corrosive limit specified for each corrosive substance to which is assigned phrase R 35 expressed as a percentage by weight.

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PC, R 35 is the percentage by weight of each corrosive substance to which is assigned phrase R 35 in the preparation. PC, R 34 is the percentage by weight of each corrosive substance to which is assigned phrase R 34 in the preparation. LC, R 34 is the corrosive limit specified for each corrosive substance to which is assigned phrase R 34 expressed as a percentage by weight. PXi, R 41 is the percentage by weight of each irritant substance to which is assigned phrase R 41 in the preparation.

LXi, R 41 is the irritant limit specified for each irritant substance to which is assigned phrase R 41 expressed as a percentage by weight.Having regard to the Treaty establishing the European Economic Community, and in particular Article a thereof.

Whereas measures should be adopted in the context of the internal market; whereas the internal market is an area without internal frontiers in which the free movement of goods, persons, services and capital is ensured. Whereas the content and scope of the laws, regulations and administrative provisions in force in the Member States with regard to the safety, health protection and performance characteristics of medical devices are different; whereas the certification and inspection procedures for such devices differ from one Member State to another; whereas such disparities constitute barriers to trade within the Community.

Whereas the national provisions for the safety and health protection of patients, users and, where appropriate, other persons, with regard to the use of medical devices should be harmonized in order to guarantee the free movement of such devices within the internal market. Whereas the harmonized provisions must be distinguished from the measures adopted by the Member States to manage the funding of public health and sickness insurance schemes relating directly or indirectly to such devices; whereas, therefore, the provisions do not affect the ability of the Member States to implement the abovementioned measures provided Community law is complied with.

Whereas medical devices should provide patients, users and third parties with a high level of protection and attain the performance levels attributed to them by the manufacturer; whereas, therefore, the maintenance or improvement of the level of protection attained in the Member States is one of the essential objectives of this Directive. Whereas, in accordance with the principles set out in the Council resolution of 7 May concerning a new approach to technical harmonization and standardization, rules regarding the design and manufacture of medical devices must be confined to the provisions required to meet the essential requirements; whereas, because they are essential, such requirements should replace the corresponding national provisions; whereas the essential requirements should be applied with discretion to take account of the technological level existing at the time of design and of technical and economic considerations compatible with a high level of protection of health and safety.

Whereas, in order to demonstrate conformity with the essential requirements and to enable conformity to be verified, it is desirable to have harmonized European standards to protect against the risks associated with the design, manufacture and packaging of medical devices; whereas such harmonized European standards are drawn up by private-law bodies and should retain their status as non-mandatory texts; whereas, to this end, the European Committee for Standardization CEN and the European Committee for Electrotechnical Standardization Cenelec are recognized as the competent bodies for the adoption of harmonized standards in accordance with the general guidelines on cooperation between the Commission and these two bodies signed on 13 November.

Whereas in cases where the conformity of the devices can be assessed under the responsibility of the manufacturer the competent authorities must be able, particularly in emergencies, to contact a person responsible for placing the device on the market and established in the Community, whether the manufacturer or another person established in the Community and designated by the manufacturer for the purpose.

Whereas medical devices should, as a general rule, bear the CE mark to indicate their conformity with the provisions of this Directive to enable them to move freely within the Community and to be put into service in accordance with their intended purpose. Whereas, in the fight against AIDS and in the light of the conclusions of the Council adopted on 16 May regarding future activities on AIDS prevention and control at Community level, medical devices used for protection against the HIV virus must afford a high level of protection; whereas the design and manufacture of such products should be verified by a notified body.

Whereas the confirmation of complicance with the essential requirements may mean that clinical investigations have to be carried out under the responsibility of the manufacturer; whereas, for the purpose of carrying out the clinical investigations, appropriate means have to be specified for the protection of public health and public order.

Whereas the protection of health and the associated controls may be made more effective by means of medical device vigilance systems which are integrated at Community level. This Directive shall apply to medical devices and their accessories. For the purposes of this Directive, accessories shall be treated as medical devices in their own right.

Both medical devices and accessories shall hereinafter be termed devices. The relevant essential requirements of Annex I to this Directive shall apply as far as safety and performance-related device features are concerned.

The devices must meet the essential requirements set out in Annex I which apply to them, taking account of the intended purpose of the devices concerned.

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Member States shall not create any obstacle to the placing on the market or the putting into service within their territory of devices bearing the CE marking provided for in Article 17 which indicate that they have been the subject of an assessment of their conformity in accordance with the provisions of Article At trade fairs, exhibitions, demonstrations, etc.Avis juridique important. Having regard to the Treaty establishing the European Economic Community, and in particular Article 75 thereof.

Whereas the obligation to use such recording equipment can be imposed only for vehicles registered in Member States; whereas furthermore certain of such vehicles may, without giving rise to difficulty, be excluded from the scope of this Regulation. Whereas the Member States should be entitled, with the Commission's authorization, to grant certain vehicles exemptions from the provisions of the Regulation in exceptional circumstances; whereas, in urgent cases, it should be possible to grant these exemptions for a limited time without prior authorization from the Commission.

Whereas, in order to ensure effective checking, the equipment must be reliable in operation, easy to use and designed in such a way as to minimize any possibility of fraudulent use; whereas to this end recording equipment should in particular be capable of providing, on separate sheets for each driver and in a sufficiently precise and easily readable form, recorded details of the various periods of time.

Whereas automatic recording of other details of a vehicle's journey, such as speed and distance covered, will contribute significantly to road safety and will encourage sensible driving of the vehicle; whereas, consequently, it appears appropriate to provide for the equipment also to record those details.

Whereas it is necessary to set Community construction and installation standards for recording equipment and to provide for an EEC approval procedure, in order to avoid throughout the territory of the Member States any impediment to the registration of vehicles fitted with such recording equipment, to their entry into service or use, or to such equipment being used.

Whereas, in the event of differences of opinion between Member States concerning cases of EEC type approval, the Commission should be empowered to take a decision on a dispute within six months if the States concerned have been unable to reach a settlement.

article eec number sheet dimensions

Whereas it would be helpful in implementing this Regulation and preventing abuses to issue drivers who so request with a copy of their record sheets. Whereas, in order to achieve the aims hereinbefore mentioned of keeping a check on work and rest periods, it is necessary that employers and drivers be responsible for seeing that the equipment functions correctly and that they perform with due care the operations prescribed.

Whereas the provisions governing the number of record sheets that a driver must keep with him must be amended following the replacement of the flexible week by a fixed week. Whereas technical progress necessitates rapid adaptation of the technical specifications set out in the Annexes to this Regulation; whereas, in order to facilitate the implementation of the measures necessary for this purpose, provision should be made for a procedure establishing close cooperation between the Member States and the Commission within an Advisory Committee.

Whereas, in order to ensure that recording equipment functions reliably and correctly, it is advisable to lay down uniform requirements for the periodic checks and inspections to which the equipment is to be subject after installation.

Recording equipment within the meaning of this Regulation shall, as regards construction, installation, use and testing, comply with the requirements of this Regulation and of Annexes I and II thereto, which shall form an integral part of this Regulation. Member States shall inform the Commission of any exemption granted under this paragraph. In urgent cases they may grant a temporary exemption for a period not exceeding 30 days, which shall be notified immediately to the Commission.

The Commission shall notify the other Member States of any exemption granted pursuant to this paragraph. In the case of national transport operations, Member States may require the installation and use of recording equipment in accordance with this Regulation in any of the vehicles for which its installation and use are not required by paragraph 1.

Applications for EEC approval of a type of recording equipment or of a model record sheet shall be submitted, accompanied by the appropriate specifications, by the manufacturer or his agent to a Member State.

No application in respect of any one type of recording equipment or of any one model record sheet may be submitted to more than one Member State.OJ L Avis juridique important. Having regard to the Treaty establishing the European Economic Community, and in particular Article 75 thereof.

Whereas the obligation to use such recording equipment can be imposed only for vehicles registered in Member States; whereas furthermore certain of such vehicles may, without giving rise to difficulty, be excluded from the scope of this Regulation. Whereas the Member States should be entitled, with the Commission's authorization, to grant certain vehicles exemptions from the provisions of the Regulation in exceptional circumstances; whereas, in urgent cases, it should be possible to grant these exemptions for a limited time without prior authorization from the Commission.

Whereas, in order to ensure effective checking, the equipment must be reliable in operation, easy to use and designed in such a way as to minimize any possibility of fraudulent use; whereas to this end recording equipment should in particular be capable of providing, on separate sheets for each driver and in a sufficiently precise and easily readable form, recorded details of the various periods of time.

Whereas automatic recording of other details of a vehicle's journey, such as speed and distance covered, will contribute significantly to road safety and will encourage sensible driving of the vehicle; whereas, consequently, it appears appropriate to provide for the equipment also to record those details. Whereas it is necessary to set Community construction and installation standards for recording equipment and to provide for an EEC approval procedure, in order to avoid throughout the territory of the Member States any impediment to the registration of vehicles fitted with such recording equipment, to their entry into service or use, or to such equipment being used.

Whereas, in the event of differences of opinion between Member States concerning cases of EEC type approval, the Commission should be empowered to take a decision on a dispute within six months if the States concerned have been unable to reach a settlement. Whereas it would be helpful in implementing this Regulation and preventing abuses to issue drivers who so request with a copy of their record sheets.

Whereas, in order to achieve the aims hereinbefore mentioned of keeping a check on work and rest periods, it is necessary that employers and drivers be responsible for seeing that the equipment functions correctly and that they perform with due care the operations prescribed. Whereas the provisions governing the number of record sheets that a driver must keep with him must be amended following the replacement of the flexible week by a fixed week.

Whereas technical progress necessitates rapid adaptation of the technical specifications set out in the Annexes to this Regulation; whereas, in order to facilitate the implementation of the measures necessary for this purpose, provision should be made for a procedure establishing close cooperation between the Member States and the Commission within an Advisory Committee.

Whereas, in order to ensure that recording equipment functions reliably and correctly, it is advisable to lay down uniform requirements for the periodic checks and inspections to which the equipment is to be subject after installation. Recording equipment within the meaning of this Regulation shall, as regards construction, installation, use and testing, comply with the requirements of this Regulation and of Annexes I and II thereto, which shall form an integral part of this Regulation.

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Member States shall inform the Commission of any exemption granted under this paragraph. In urgent cases they may grant a temporary exemption for a period not exceeding 30 days, which shall be notified immediately to the Commission.

The Commission shall notify the other Member States of any exemption granted pursuant to this paragraph. In the case of national transport operations, Member States may require the installation and use of recording equipment in accordance with this Regulation in any of the vehicles for which its installation and use are not required by paragraph 1.

Applications for EEC approval of a type of recording equipment or of a model record sheet shall be submitted, accompanied by the appropriate specifications, by the manufacturer or his agent to a Member State.

No application in respect of any one type of recording equipment or of any one model record sheet may be submitted to more than one Member State. A Member State shall grant EEC approval to any type of recording equipment or to any model record sheet which conforms to the requirements laid down in Annex I to this Regulation, provided the Member State is in a position to check that production models conform to the approved prototype. Any modifications or additions to an approved model must receive additional EEC type approval from the Member State which granted the original EEC type approval.

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Member States shall issue to the applicant an EEC approval mark, which shall conform to the model shown in Annex II, for each type of recording equipment or model record sheet which they approve pursuant to Article 5. The competent authorities of the Member State to which the application for type approval has been submitted shall, in respect of each type of recording equipment or model record sheet which they approve or refuse to approve, either send within one month to the authorities of the other Member States a copy of the approval certificate accompanied by copies of the relevant specifications, or, if such is the case, notify those authorities that approval has been refused; in cases of refusal they shall communicate the reasons for their decision.

If a Member State which has granted EEC type approval as provided for in Article 5 finds that certain recording equipment or record sheets bearing the EEC type approval mark which it has issued do not conform to the prototype which it has approved, it shall take the necessary measures to ensure that production models conform to the approved prototype.

The measures taken may, if necessary, extend to withdrawal of EEC type approval.Sign In. Join Free. Inquiry Basket. Get Apps. Post Sourcing Request. Jinhua Easyway Technology Co.

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article eec number sheet dimensions

Diamond Member Since Audited Supplier. Print This Page. Favorites Favorites Share. Get Latest Price. Port: Ningbo, China.How to calculate package size and weight, and definition of dimensional weight pricing. Additional Information. Maximum Parcel Size. How can I determine the weight of a package? The U. Please keep in mind that if the package weighs more than the weight you entered, it will require additional postage when it is mailed or delivered. For one low price, you can mail any amount of material to a U.

Maximum Parcel Weight. What is Dimensional-Weight Pricing? Dimensional-weight pricing is based on the cubic capacity of a package parcel rather than the weight.

It converts the cubic size of an item into a dimensional weight. If a large package is relatively light, it could be charged as a heavier-weight item based on a standard issued by the International Air Transport Association IATA.

This standard is used by other commercial carriers to determine prices for packages shipped by air and it aligns to Priority Mail prices with the expense incurred for shipping these items by air. More information on dimensional-weight pricing can be found at What are the Different Ways Parcels are Priced?

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Directive 67/548/EEC

How can we help? Search for a topic.OJ Avis juridique important. Having regard to the Treaty establishing the European Economic Community, and in particular Article thereof. Whereas any rules concerning the placing on the market of dangerous substances and preparations must aim at protecting the public, and in particular workers using such substances and preparations.

Whereas the differences between the national provisions of the six Member States on the classification, packaging and labelling of dangerous substances and preparations hinder trade in these substances and preparations within the Community and hence directly affect the establishment and functioning of the common market.

Whereas it is therefore necessary to remove such hindrances ; whereas this entails approximating the laws, regulations and administrative provisions on classification, packaging and labelling. Whereas, in view of the preparatory work still to be carried out, the approximation of provisions relating to dangerous preparations will have to be dealt with in later directives ; whereas therefore the present Directive must be restricted to the approximation of provisions relating to dangerous substances.

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Whereas in view of the extent of this field and the many detailed measures which will be required for the approximation of all the provisions relating to dangerous substances, it would appear advisable to deal first with the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances and to deal in later directives with the approximation of the provisions relating to the use of those dangerous substances and preparations if it is established that the differences between such provisions directly affect the establishment or functioning of the common market.

Whereas the approximation of national provisions which is laid down by this Directive does not prejudice application of the provisions of Articles 31 and 32 of the Treaty. The purpose of this Directive is to approximate the laws, regulations and administrative provisions of the Member States on: - classification.

This Directive does not affect the provisions relating to: a medicinal products, narcotics and radioactive substances ; 1 OJ NoArticles 5 to 7 of this Directive do not apply to containers for gases which are compressed, liquefied or dissolved under pressure. The following substances and preparations are "dangerous" within the meaning of this Directive: a explosive:.

The classification of dangerous substances according to the greatest degree of hazard and specific nature of the risks shall be based on the categories laid down in Article 2. Annex I to this Directive gives the list of dangerous substances classified in accordance with the provisions of Article 3. Member States shall take all necessary measures to ensure that dangerous substances cannot be placed on the market unless the strength and impermeability of their packaging satisfies the following requirements, any packaging meeting these requirements being regarded as adequate: 1.

The packagings must be so arranged and fastened as to preclude any loss of the contents ; this requirement does not apply where special safety devices are prescribed.

The materials constituting the packaging and fastenings must not be liable to attack by the contents, or liable to form harmful or dangerous compounds with the contents. The packagings and fastenings must be strong and solid throughout to ensure that they will not loosen and will safely meet the normal stresses and strains of handling. Member States shall take all necessary measures to ensure that dangerous substances cannot be placed on the market unless the labelling on their packaging satisfies the following requirements.

The symbols must conform to those in Annex II to this Directive ; they shall be printed in black on an orange-yellow background. If the packaging is accompanied by advice on safety precautions relating to the use of the substances, the wording of this shall, in conformity with the references contained in the list in Annex I, be taken from Annex IV to this Directive.

Where the particulars required by Article 6 appear on a label, that label must be placed on one or more surfaces of the packaging so that it can be read horizontally when the package is set down normally.


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