1. Initial type testing

    1. Initial type testing shall be performed to demonstrate conformity with this European Standard.

All characteristics given in clauses 4, 5 and 6 shall be subject to this initial type testing, except as described in 10.2.3 to 10.2.5.

  1. In the case of modification of the component or of the method of production (where these may affect the stated properties), initial type testing shall be performed. All characteristics given in clauses 4, 5 and 6, which may be changed by the modification, shall be subject to this initial type testing, except as described in 10.2.3 to 10.2.5.

  2. Tests previously performed in accordance with the provisions of this standard may be taken into account providing that they were made to the same or a more rigorous test method under the same system of attestation of conformity on the same component or components of similar design, construction and functionality, such that the

. up^hvwuiv i.w uiu Uvii^VHviH 4UVUUUH.

NOTE Same system of attestation of conformity means testing by an independent third party under the control of a product certification body.

  1. Components may be grouped into families where one or more characteristics are the same for all components within that family or the test results are representative of all components within that family. In this case not all components of the family have to be tested for the purposes of the initial type testing.

  2. Where the characteristics of the component have previously been demonstrated according to the requirements of EN 54-2, EN 54-4 and EN 60529, no further evaluation of the component, in respect of these characteristics, is required to show Conformity with this European Standard.

  3. Test samples shall be representative of the normal production. If the test samples are prototypes, they shall be representative of the intended future production and shall be selected by the manufacturer.

NOTE In the case of prototypes and third party certification, this means that it is the manufacturer not the third party who is responsible for selecting the samples. During the initial inspection of the factory and of the factory production control (see 10.3), it is verified that the component continuously complies with the initial type testing samples.

    1. If the technical documentation of the test samples does not give a sufficient basis for later compliance checks, a reference sample (identified and marked) shall remain available for this purpose.

    2. Any initial type testing and its results shall be documented in a test report.

  1. Factory production control (FPC)

    1. Genera!

The manufacturer shall establish, document and maintain an FPC system to ensure that the components placed on the market conform with the stated performance characteristics.

If the manufacturer has the component designed, manufactured, assembled, packed, processed and labelled by subcontracting, FPC of the subcontractor may be taken into account. Where subcontracting takes place, the manufacturer shall retain the overall control of the component and ensure that he receives all the information that is necessary to fulfil his responsibilities according to this European Standard. The manufacturer who subcontracts all of his activities may in no circumstances discharge himself of his responsibilities to a subcontractor.

FPC is the permanent internal control of production exercised by the manufacturer.

All the elements, requirements and provisions adopted by the manufacturer shall be documented in a systematic manner in the form of written policies and procedures. This production control system documentation shall ensure a common understanding of conformity evaluation and enable the achievement of the required component characteristics and the effective operation of the production control system to be checked.

Factory production control therefore brings together operational techniques and all measures allowing maintenance and control of the conformity of the component with its technical specifications. Its implementation may be achieved by controls and tests on measuring equipment, raw materials and constituents, processes, machines and manufacturing equipment and finished components, including material properties in components, and by making use of the results thus obtained.

  1. General requirements

The FPC system should fulfil the requirements as described in the following clauses of EN ISO 9001:2000, where applicable:

— 4.2 except 4.2.1 a)

— 5.1 e), 5.5.1, 5.5.2

— clause 6

— 7.1 except 7.1 a), 7.2.3 c), 7.4, 7.5, 7.6

— 8.2.3, 8.2.4, 8.3, 8.5.2

The FPC system may be part of a Quality Management system, e.g. in accordance with EN ISO 9001.

  1. Component specific requirements

    1. The FPC system shall

  • address this European Standard; and

  • ensure that the components placed on the market conform with the stated performance characteristics.

  1. The FPC system shall include a component specific FPC- or Quality-plan, which identifies procedures to demonstrate conformity of the component at appropriate stages, i.e.

  1. the controls and tests to be carried out prior to and/or during manufacture according to a frequency laid down; and/or

  2. the verifications and tests to be carried out on finished components according to a frequency laid down.

If the manufacturer uses finished components, the operations under b) shall lead to an equivalent level of conformity of the component as if normal FPC had been carried out during the production.

If the manufacturer carries out parts of the production himself, the operations under b) may be reduced and partly replaced by operations under a). Generally, the more parts of the production are carried out by the manufacturer, the more operations under b) may be replaced by operations under a). In any case the operation shall lead to an equivalent level of conformity of the component as if normal FPC had been carried out during the production.

NOTE Depending on the specific case, it can be necessary to carry out the operations referred to under a) and b), only the operations under a) or only those under b).

The operations under a) centre as much on the intermediate states of the component as on manufacturing machines and their adjustment, and measuring equipment etc. These controls and tests and their frequency are chosen based on component type and composition, the manufacturing process and its complexity, the sensitivity of component features to variations in manufacturing parameters etc.

The manufacturer shall establish and maintain records which provide evidence that the production has been sampled and tested. These records shall show clearly whether the production has satisfied the defined acceptance criteria and shall be available at least for ten years. Where the component fails to satisfy the acceptance measures, the provisions for non-conforming products shall apply, the necessary corrective action shall immediately be taken and the components or batches not conforming shall be isolated and properly identified. Once the fault has been corrected, the test or verification in question shall be repeated.

The results of controls and tests shall be properly recorded. The component description, date of manufacture, test method adopted, test results and acceptance criteria shall be entered in the records under the signature of the person responsible for the control/test. With regard to any control result not meeting the requirements of this European Standard, the corrective measures taken to rectify the situation (e.g. a further test carried out, modification of manufacturing process, throwing away or putting right of the component) shall be indicated in the records.

    1. Individual components or batches of components and the related manufacturing documentation shall be completely identifiable and retraceable.

  1. Initial inspection of factory and FPC

    1. Initial inspection of factory and FPC shall generally be carried out when the production is already running ano uie rru is анеаоу in piacuce. it is, however, possible, that the iniual inspection of factory and FPC is carried out before the production is already running and/or before the FPC is already in practice.

    2. The following shall be assessed to verify that the requirements of 10.3.2 and 10.3.3 are fulfilled:

  • the FPC-documentation; and

  • the factory.

In the assessment of the factory it shall be verified:

  1. that all resources necessary for the achievement of the component characteristics required by this European Standard are or will be (see 10.3.4.1) available; and

  2. that the FPC-procedures in accordance with the FPC-documentation are or will be (see 10.3.4.1) implemented and followed in practice; and

  3. that the component complies or will comply (see 10.3.4.1) with the initial type testing samples, for which compliance with this European Standard has been verified; and

  4. whether the FPC system is part of a Quality Management system in accordance with EN ISO 9001 (see 10.3.2) and as part of this Quality Management system is certified and has yearly surveillance by a certification body, who is recognised by an accreditation body which is member of the "European Co-operation for Accreditation” and which has signed the “Multilateral agreement’ (MLA) there.

  1. All factories of the manufacturer, where for the relevant component final assembling or at least final testing is performed, shall be assessed to verify that the conditions of 10.3.4.2 a) to c) are in place. One assessment may cover one or more components, production lines and/or production processes. If the FPC system covers more than one component, production line or production process, and if it is verified that the general requirements are fulfilled then the detailed verification of the component specific FPC requirements for one component may be taken as representative of the FPC of other components.

  2. Assessments previously performed in accordance with the provisions of this standard may be taken into account providing that they were made to the same system of attestation of conformity on the same component or components of similar design, construction and functionality, such that the results may be considered applicable to the component in question.

NOTE Same system of attestation of conformity means inspection of FPC by an independent third party under the control of a product certification body.

    1. Any assessment and its results shall be documented in a report.

  1. Continuous surveillance of FPC

    1. All factories which have been assessed according to 10.3.4 shall be re-assessed once a year, except as stated in 10.3.5.2.

In this case each FPC assessment shall verify a different component or production process, where applicable.

  1. If the manufacturer provides proof of continuing satisfactory operation of his FPC system the frequency of the re-assessment may be reduced to once every four years.

NOTE 1 Sufficient proof can be the report of a certification body, see 10.3.4.2 d).

NOTE 2 If the overall Quality Management system in accordance with EN ISO 9001 is well implemented (verified in the initial assessment of factory and FPC) and continuously practised (verified in QM-audits), it can be assumed that the integrated FPC- relevant part is well covered. On this basis, the work of the manufacturer is well controlled, so that the frequency of special FPC- surveillance-assessments can be reduced.

    1. Any assessment and its results shall be documented in a report.

  1. Procedure for modifications

In the case of modification of the component, the method of production or the FPC system (where these may affect the stated properties), a re-assessment of the factory and of the FPC system shall be performed for those aspects which may be affected by the modification.

Any assessment and its results shall be documented in a report.



Annex A

(normative)

Summary of indications

A summary of indications is shown in Table A.1.

Table A.1 — Indications

Information

Indication

A

Visible

Special conditions

L

L/D

per

AL

Colour

e.c.d. is supplied with power

mmm

X

МММ

e.c.d

1

green


Activated condition

X

X

МММ

f.z.

1

red

4.9.3 (two alarm signals)

Released condition

mmm

X

МММ

f.z.

1

red

МММ

Transmission 'Released condition’

a ■“

X

e.c.d

1

red

4.3.2 f) (output specified for EN 54-1 (E))

Fault warning condition

Fault in t.p. to an f.d.a.s. or inside the fire extinguishing system

X

:

X

f.z.

1

yellow

4.14.10 (No suppression). 4.14.1 b) (faults related to more than 1 f.z.). 4.20 (emergency hold 2 s).

X

X

t.p.

1, 2 or

3

yellow

Fault in t.p. to J or E (EN 54-1)

X

MmM

X

t.p.

1

yellow

МММ

Power supply fault, faults of p.s.e. as described in EN 54-4 and fault of t.p. between e.c.d. and p.s.e.

X

X

e.c.d

1

yellow

4.13.1 j) 2) (t.p. not inside the cabinet(s) of the e.c.d. or p.s.e. more than 0,1 m)

Earth fault affecting the function of the e.c.d.

X

МММ

X

e.c.d

1

yellow

4.14.5 (visible indication only required, if not covered by another fault indication)

Rupture of fuse or operation of protective device, preventing the operation of the e.c.d.

X

X

e.c.d

1

yellow

4.14.6 (visible indication at least as fault indication for the supervised function)

Incorrect execution of program and/or corruption of memory content (only for software controlled e.c.d.)

X

X

—-

f.z.

or e.c.d

1

yellow

4.14.7 (indication until manual reset and/or another manual operation), 6.3.1 (program)

Common fault

X

X

МММ

e.c.d.

1

yellow

5.3.1

Additional conditions for fault warning indications

4.14.8/4.14.9 (indication of faults, detected but not displayed because of limited space of display).

4.14.13 (output to transmit information of the fault warning condition, even if e.c.d. is deenergized).

Disabled condition

mmm

X

X

f.z.

1

yellow

МММ

Monitoring (e.g. incorrect status of components, loss of agent)

X

МММ

X

МММ

1

yellow

4.19.2 (activation of output ‘fault condition’)

Separate monitoring of non-electrical disable device, indication of blocked position

X

X

-мм

f.z.

1

yellow

separate indication of blocked position and also fault indication, see 4.19.3 (output), (indication of incorrect position), (activation of output ‘fault condition’)

Manual only mode

МММ

X

f.z.

1

yellow

4.23 (output to transmit the information about this mode)

Emergency hold device activated

X

X

МММ

f.z.

1

yellow

4.20 (indication until manual reset), (output)

Emergency abort device activated

X

X

МММ

f.z.

1

yellow

4.27 (indication until manual reset), (output)

Spare bank activation at next alarm

mmm

МММ

X

Bank

1

yellow

МММ

Key:

A: Audible indication by audible indicator (internal buzzer)

L: Visible indication by a separate light emitting indicator

L/D: Visible indication by a separate light emitting indicator or by an alphanumeric display

AL: Access level

Colour: Colour of separate light emitting indicator

f.z.: Flooding zone

t.p.: Transmission path

Annex В
(informative)

Design requirements for software controlled e.c.d.

If a failure of program execution is detected, as specified in 6.3.1, the e.c.d. enters a safe state, as defined by the manufacturer. It is expected that this safe state will not result in the false actioning of compulsory outputs, nor give a false impression to a user that the e.c.d. remains operational if it is not.

It is accepted either to stop, or to automatically attempt to restart, the program execution. If there is a risk that memory may have been corrupted, the restart procedure should check the contents of the memories, and if necessary re-initialize running data to ensure that the e.c.d. enters a safe operating state.

Even if program execution is successfully restarted, it is important that the user is made aware of the incident. For this reason it can be advantageous if the e.c.d. is capable of automatically recording details of the restart event. In any event the fault indication of the failure of program execution will be latched until a manual intervention.

6.4.1 requires that all executable code and data necessary to comply with this standard will be held in memory which is capable of continuous, unmaintained, reliable operation for a period of at least 10 years. In the existing state of the art, memory with moving mechanical parts is not believed to be sufficiently reliable. The use of tapes, or magnetic or optical data discs for the storage of programs and data is therefore not recommended at the time of drafting this standard.Annex ZA

(informative)

Clauses of this European Standard addressing the provisions of the EU
Construction Products Directive

ZA.O Scope of this annex

The scope as given in clause 1 is applicable.

ZA.1 Relationship between EU Directive and this European Standard

This European Standard has been prepared under a Mandate given to CEN by the European Commission and the European Free Trade Association.

The clauses of this European Standard shown in this annex meet the requirements of the Mandate given under the EU Construction Products Directive (89/106).

Compliance with these clauses confers a presumption of fitness of the construction products covered by this European Standard for their intended use.

WARNING — Other requirements and other EU Directives, not affecting the fitness for intended use may be applicable to a construction product falling within the scope of this standard.