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The CE Mark

The CE mark is a mandatory conformity mark on many products placed on the single market in the European Economic Area (EEA).

By affixing the CE marking, the manufacturer, its authorized representative, or person placing the product on the market or putting it into service asserts that the item meets all the essential requirements of all applicable EU directives and that the applicable conformity assessment procedures have been applied. Examples of European Directives requiring CE marking include toy safety, machinery, low-voltage equipment, EM compatibility. There are about 25 Directives requiring CE marking.

The CE marking is a mandatory European marking for certain product groups to indicate conformity with the essential health and safety requirements set out in European Directives. To permit the use of a CE mark on a product, proof that the item meets the relevant requirements must be documented. Sometimes this is achieved using an external test house which evaluates the product and its documentation. Often it is achieved by a company-internal self-certification process.

In any case the responsible organization (manufacturer, representative, importer) has to issue a EC-Declaration of Conformity (EC-DoC) indicating his identity (location, etc.), the list of European Directives he declares compliance with, a list of standards the product complies with, and a legally binding signature on behalf of the organization. The EC-DoC underlines the sole responsibility of the manufacturer. Parts of the certification process for the CE marking could be performed by 3rd party test houses or certification bodies; in case that this is mandatory the CE symbol also includes a number that identifies the so called Notified Body.

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KEYPAD
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The FCC Mark

The FCC's Office of Engineering and Technology operates the Equipment Authorization Branch, which is tasked with overseeing equipment authorization for all devices using the electromagnetic energy from 9 kHz to 300 GHz. OET maintains an electronic database of all Certified equipment which can be easily accessed by the public.

A Declaration of Conformity is a procedure where the responsible party as defined in Section 2.909, makes measurements or takes other necessary steps to ensure that the equipment complies with the appropriate technical standards. Submittal of a sample unit or representative data to the Commission demonstrating compliance is not required unless specifically requested pursuant to Section 2.1076.

Devices must be tested by a test laboratory accredited by the National Voluntary Laboratory Accreditation Program (NVLAP); the American Association of Laboratory Accreditation (A2LA); or an accredited laboratory designated by the Commission under the terms of a negotiated Mutual Recognition Agreement (MRA).

The ISO9001 Mark

ISO 9001:2000 is intended for use in any organization which designs, develops, manufactures, installs and/or services any product or provides any form of service. It provides a number of requirements which an organization needs to fulfill if it is to achieve customer satisfaction through consistent products and services which meet customer expectations.

Report
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Declaration
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The UL RoHS Mark

The UL RoHS program requires initial testing of representative samples down to the homogeneous material level for six restricted substances. The program participants set the limits below which they undertake to maintain the levels of the six restricted substances. These limits must be below the UL-RoHS program limits in parts-per-million (ppm):

The program operates a twice-a-year surveillance process consisting of:

• A quality management system audit.
• A product review.
• Collection of samples materials for testing. The program tests samples of customer's product to the homogeneous substance level for all restricted substances in no more than a two-year cycle.

Those products that have been found to meet the requirements of the program are included in iQ for Restricted Substances, a database that is open to anyone who chooses to create an account.