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CE marking label or European Conformity certification mark. Vector EU high quality certificate seal and stars

CE marking is a Key indicator of a product’s compliance through European Union (EU) health, safety and environmental protection directives and regulations.If your product comes under the scope of a directive requiring CE marking you must ensure the product complies with the applicable requirements or fulfil the requirement of harmonized standard and affix the CE mark(Standard logo) before placing it in the market in the European Economic Area (EEA). 

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RoHS Compliance

RoHS, also known as Lead-Free, stands for Restriction of Hazardous Substances. RoHS, also known as Directive 2002/95/EC, originated in the European Union and restricts the use of six hazardous materials found in electrical and electronic products. All applicable products in the EU market after July 1, 2006 must pass RoHS compliance. RoHS impacts the entire electronics industry and many electrical products as well.

 

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Reach Compliance

REACH is a European Community (EC) Regulation that deals with the registration, evaluation, authorization and restriction of chemical substances. Effective 1st June 2007, REACH requires manufacturers and importers to register all substances they produce in /or import to the European Union in quantities ≥ 1 ton per year with the Helsinki-based European Chemicals Agency (ECHA).

About Us

KBS has Mutual Level Agreement (MLA) with Top Notified Body across Europe. KBS can assist you to gain easier access into the European market by ensuring your product meets all the CE mark requirements. If you manufacture or import products which falls under the scope of one or more of the New Approach Directives then you will need professional guidance on how to meet all the essential requirements of these directives. KBS has the capabilities and technical expertise for professional guidance.

Choose Your Directives/Regulations

machinery directive

Machinery Directive

Machinery Directive(MD) 2006/42/EC main intent is to ensure a common safety level in machinery placed on the market or put in service within the European Union.Manufacturers of equipment that fall under the scope of the directive, such as grinding machines, lathe and packaging machines, must issue a Declaration of Conformity (DoC) in order to sell their products in the EU

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Low Voltage Directives

Low Voltage Directive (LVD) 2006/95/EC is one of the oldest Single Market Directives adopted by the European Union before the “New” or “Global” Approach. The Directive provides common broad objectives for safety regulations, so that electrical equipment approved by any EU member country will be acceptable for use in all other EU countries.

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Construction Products Regulation

Construction Products Regulation, (CPR) 89/106/EEC is a regulation that lays down harmonised conditions for the manufacturing and marketing of construction products and aims to remove technical barriers .The EU regulation is designed to simplify and clarify the existing framework for the placing on the market of construction products.

Safety Equipment Isolated

Personal Protective Equipment Directive

PPE Regulation (EU) 2016/425 on personal protective equipment covers the design, manufacture and marketing of PPE. It defines legal obligations to ensure that PPE on the EU internal market provides the highest level of protection against risks. The CE marking affixed to PPE provides evidence of compliance of the product with the applicable EU legislation.

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Pressure Equipments Directive(PED)

Pressure Equipment Directive (PED) 2014/68/EU sets out the standards for the design and fabrication of pressure equipment like steam boilers, pressure vessels, piping, safety valves etc . It also sets the administrative procedures requirements for the “conformity assessment” of equipment for the free placing on the European market without local legislative barriers.

EU+MDR

Medical Devices Regulation

Medical Device Directive (MDR) 93/42/EEC ,is intended to harmonise the laws relating to medical devices within the EU .For a manufacturer to legally place a medical device on the European market, the requirements of the MD Directive have to be met. Manufacturers’ products meeting ‘harmonised standards have a presumption of conformity to the Directive.

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EMC Directive

Electromagnetic compatibility (EMC) is the ability of electrical equipment and systems to function acceptably in their electromagnetic environment, by limiting the unintentional generation, propagation and reception of electromagnetic energy which may cause unwanted effects such as electromagnetic interference (EMI) or even physical damage to it.

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Measuring Instruments Directive

Measuring Instruments Directive (MID) 2014/32/EU seeks to harmonise many aspects of legal metrology across all member states of the EU,i.e.all meters which receive a MID approval may be used in all countries across the EU. It provides options to manufacturer as to how the requirements are met and how to apply to for conformity assessment on their instrument.

Radio Equipment Directive

Radio Equipment Directive (RED, 2014/53/EU) established a regulatory framework for All radio equipment within the scope of this directive that are to be placed on the EU market .It describes essential requirements of RED to ensure protection of health and safety, adequate electromagnetic compatibility (EMC) and effective and efficient use of the radio spectrum.

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