Gas Burning Devices Inspection

a. This Regulation applies to gas-burning appliances for processes such as cooking, heating, hot water production, cooling, lighting or washing which does not exceed 105 ° C. Devices that burn gas (gas fuel) are then referred to as bundan devices Gaz. Burners and heating units with this type of burner are considered as ül devices Br. Used or sold separately in commercially available and gas-fired devices for commercial use; Safety, control or adjustment devices and semi-products other than burners or burner heating units are then referred to as ısıtma fitting br.

b. Devices specially designed for use in industrial processes in industrial areas are outside the scope defined in paragraph 1.

c. For the purpose of this regulation, ’gaseous fuel, is any gaseous fuel under pressure of 1 bar at 15 ° C.

D. For the purposes of this regulation, the dı normal use ına of a device means that the device has been correctly installed and serviced regularly according to the manufacturer’s instructions, and is used in accordance with the intended purpose for normal use of gas quality and with normal deviation from the pressure source.

Legal Status:

As of June 29, 1990, the 90/396 / EEC Gas Burning Devices Regulation (Appliances Burning Gaseous Fuels Directive) has been mandatory in the Member States. On March 19, 2003 Turkey de Gas Appliances Directive (90/396 / EC) was published and became mandatory on 1 January 2004.

Conformity Assessment Procedures

• EC Type examination (Module B) (Annex II, Article 1)
• EC Type Declaration of Conformity (Module C) (Annex II, Article 2)
• EC Type Declaration of Conformity (Module D) (Annex II, Article 3) Production Quality Assurance (ISO 9001: 2000 Article 7.3)
• EC Declaration of Type Conformity (Module E) (Annex II, Article 4) Product Quality Assurance (ISO 9001: 2000 Article 7.1 7.2.3 7.3 7.4 7.5.1 7.5.2 7.5.3)
• EC Type Verification (Module F) (Annex II Article 5) EC Unit Verification (Module G) (Annex III Article 6)

AT TYPE EXAMINATION (MODULE B)
• It is the examination and certification of a device which is a sample of the designed production and conforms to the provisions of the Regulation by a notified body.
• It is a mandatory module for products manufactured and manufactured in series.
• The EC Type Certificate is issued as a result of this review.

AT Type Declaration of Conformity (Module C)
• The EC Type-Declaration of Conformity is the manufacturer’s declaration of conformity to the type specified in the EC Type Certificate of the relevant devices and that the equipment meets the essential requirements of the Regulation.
• CE conformity mark is attached to the devices.
• The identification mark of the notified body should be placed next to the CE conformity mark.

AT Type Declaration of Conformity (Module D) Production Quality Assurance
• The manufacturer must have a quality system that ensures that it complies with the type specified in the EC Type Certificate and the basic requirements of this regulation.
• The manufacturer must declare that the devices comply with the type specified in the EC Type Certificate and the basic requirements of this regulation.
• CE conformity mark is attached to the devices.
• The identification mark of the notified body should be placed next to the CE conformity mark.
• The manufacturer is subject to EC supervision. ISO 9001: 2000 Article 7.3. The Notified Body must perform this supervision at least every 2 years. The manufacturer has to report on these surveillance.
• The manufacturer must provide documentation on the quality system for EC surveillance and information on quality records, such as inspection reports, test data, calibration data, reports on the qualifications of the relevant personnel.

AT Type Declaration of Conformity (Module E) Product Quality Assurance
• The manufacturer must have a quality system that ensures that the devices comply with the type specified in the EC Type Certificate and the basic requirements of this regulation.
• The manufacturer must declare that the devices comply with the type specified in the EC Type Certificate and the basic requirements of this regulation.
• CE conformity mark is attached to the devices.
• The identification mark of the notified body should be placed next to the CE conformity mark.
• The manufacturer is subject to EC supervision. ISO 9001: 2000 Article 7.1, 7.2.3, 7.3, 7.4, 7.5.1, 7.5.2, 7.5.3. The Notified Body must perform this supervision at least every 2 years. The manufacturer has to report on these surveillance.
• The manufacturer must provide documentation on the quality system for EC surveillance and information on quality records, such as inspection reports, test data, calibration data, reports on the qualifications of the relevant personnel.

AT VERIFICATION (MODULE F)
• The manufacturer must declare that the devices comply with the type specified in the EC Type Certificate and the basic requirements of this regulation.
• CE conformity mark is attached to the devices.
• The identification mark of the notified body should be placed next to the CE conformity mark.
• The notified body monitors the compliance of these devices with the requirements of this Regulation by examining and testing each device or by testing and testing the devices on a statistical basis.
• The notified body must give each device an identification number and issue a written certificate of conformity with the tests performed.
• Devices for statistical inspection should be grouped into identifiable heaps of units of the same model manufactured under the same conditions.
• Stacks are inspected at random intervals.
• All other products may be placed on the market, except for non-conforming products.
ATTENTION TO ME UNIT (MODULE G)
• The manufacturer must declare that the device meets the requirements of the regulation.
• CE conformity mark is attached to the devices.
• The identification mark of the notified body should be placed next to the CE conformity mark.
• The design documentation referred to in Annex IV should be submitted to the notified body.
• Appropriate examinations and tests are performed for a single device.
• If the notified body considers it necessary, the device may perform tests and examinations after it has been installed.

WHAT DOES DESIGN DOCUMENTATION CONTINUE? (Annex IV)
• General description of the device
• Conceptual designs of the device, sub-assembly group with production drawings, diagrams related to circuits
• Definitions and explanations including the operation of the device
• A list of partially or fully implemented Standards and the definition of solutions to meet Annex I when these standards are not applied
• Test reports
• Installation and operating instructions
Where appropriate:
• Approval certificates related to the equipment installed on the device
• Approvals and certifications regarding the production, inspection and monitoring methods of the device
• Fault to the assessment of the notified body