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CE Certification
home - Machinery - Low Voltage
- Pressure Equipment - ATEX
- Technical Files
Essential
Health & Safety Requirements - Machinery
Lifecycle - Manual Handling
- Safety Of Control Systems
Here, we will take each section of the Machinery Directives and
tease them out in an attempt to expose as many variables as possible.
The original Machinery Directive, 89/392/EEC was the foundation
of essential health and safety requirements for work equipment within
the European Union. This original Directive has been amended by
Council Directives 91/368/EEC, 93/44/EEC and 98/37/EC, each of these
subsequent amendments adding new and specific requirements for work
equipment.
Some manufacturers, suppliers or users have attempted to use the
context of the Directive to fit their own products, when in fact
they should be using the spirit of the Directive to identify how
close or how far their product is to the essential health and safety
requirements as laid down in the Annexes of the Directive. Since
the Harmonised Standard EN 292-2: 1991 is literally taken straight
from Annex I of the Machinery Directive and that this standard is
one of two "A" type standards, it is the author's intention
to use EN 292-2: 1991 as a template to compliance with the Machinery
Directive. Each section of the Directive will be expanded using
references contained in both "B" and "C" class
standards as required.
Responsibility for compliance with the Machinery Directive initially
rests with the manufacturer or the authorised representative within
the EU, i.e. the people first responsible for placing the machinery
on the market. If, however, no such compliance exists then the responsibility
rests with the person putting the machinery into service, i.e. the
user/employer.
The Machinery Directive requires all new equipment installed or
put into service after 1 January 1995 to be compliant with the essential
health and safety requirements as found in Annex I of the Directive.
This includes second-hand equipment first put into service within
the European Union that emanates from countries outside of the European
Union, e.g. Japan, USA, Korea etc.
Compliance procedures have already been dealt with in Chapter 2,
therefore, in this chapter, we will deal with the core of compliance.
It should be noted at this point that there is a distinct relationship
between the contents of Annex I of the Machinery Directive, EN 292-2:
1991 and national legislation. However, as the reader covers the
entire chapter, this relationship will become apparent.
An important comment made by the author in preliminary observations
is that the manufacturer is under an obligation to assess the hazards
in order to identify all those that apply to his machine and he
must then design and construct it taking this assessment into account.
This is a clear and unambiguous statement that a risk assessment
must be made at the design stage, most probably a Preliminary Hazard
Assessment (PHA) and that of the categorisation as required by EN
954-1: 1996.
Scope Of The Directive
The field of application of the Directive is based upon
a general definition of the term "machinery" so as
to allow the technical development of products. The development
of complex installations and the risks they present are of an
equivalent nature to "machinery" that their express
inclusion in the Directive is justified. The Directive also
covers safety components that are placed on the market separately,
the safety function of which is declared by the manufacturer
or their authorised representative established in the community.
Machinery exhibited at trade fairs and exhibitions do not require
CE certification. However, viewers must be informed of its non-compliance
and that it cannot be purchased in this condition.
At some time during the machine's lifecycle, the operator decides
to short circuit the safety system by easily defeating the guard
doors. The machine can now operate with the guard doors open and
the operator receives crushing injuries to his/her hands.
The employer may still be liable if he was aware of the bad practice
and the employee is most certainly contributory to his injuries,
however, the manufacturer's may also be liable since it is their
duty to ensure that the machine is designed to operate safely throughout
it's lifecycle even under unforeseen abnormal circumstances and
that safety interlocks should not be easily bypassed.
JGMA have a vast amount of experience in the CE certification
process, including risk assessment, construction of Technical
Files, Harmonised Standards and correlating machinery between
the various Directives.
CE Certification
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