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Medical Device Regulation 2017/745
Lift certification 2014/33/EU
2014/33/EU Lift and Lift Components Safety Directive (95/16/EC)
ANNEX VB - MODUL B - AT Format Test
ANNEX XII – MODUL E – Product quality assurance for lifts
ANNEX XIV – MODUL D – Quality Assurance for Lifts
ANNEX XIII - MODUL H – Total quality assurance for lifts
ANNEX X - MODUL G – Unit Verification
ANNEX VI - MODUL F – ELEVATOR INSPECTION
a) All electric elevators;
b) CE marking and product certification for all hydraulic lifts;
CE Conformity Marking: Marking means that the manufacturer must fulfil all obligations based on the technical regulations and on the product being subject to any conformity assessment.
Technical Documentation: Technical documentation includes information on records and documents that indicate that a product has been manufactured in compliance with technical regulations and has been designed, produced and operated appropriately.
Lift Directive: The Lift Directive sets out basic health and safety requirements for lifts transporting people, people and loads or loads, ensuring that the equipment is safe before it enters the market.
The CE in CE marking consists of:
For CE conformity marking, it is necessary to minimize and maximize the marking for measurement as shown in the diagram above.
The CE marking must be identical in shape along the vertical dimension.
The vertical size must be less than 5 mm, as this minimum size may override small security features.
Lifts (of all types) must be CE marked with the number of the notified body.
