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Directives or Regulations and Standards

Directive n. Acronym Subject of directive/regulation Scope Directive PDF Official Journal PDF
2014/53/EU RED Radio equipment   VIEW   VIEW
2014/30/EU EMC Electromagnetic compatibility   VIEW   VIEW
2014/35/EU LVD Low voltage   VIEW   VIEW
2011/65/EU ROHS Restriction of the use of certain hazardous substances   VIEW   VIEW
2006/42/EC MD Machinery   VIEW   VIEW
(EU) 2023/1230 MR Machinery Regulation   VIEW   VIEW
(EU) 2017/745 MDR Medical devices Regulation   VIEW   VIEW
93/42/EEC MDD Medical devices   VIEW   VIEW
90/385/EEC AIMDD Active implantable medical devices   VIEW   VIEW
(EU) 2017/746 IVDR In vitro diagnostic medical devices Regulation   VIEW   VIEW
98/79/EC IVDD In vitro diagnostic medical devices   VIEW   VIEW
2014/68/EU PED Pressure equipment   VIEW   VIEW
2014/29/EU SPVD Simple pressure vessels   VIEW   VIEW
(EU) 2019/945 UAD Unmanned aircraft systems   VIEW   VIEW
2013/53/EU RC Recreational Craft   VIEW   VIEW
2014/34/EU ATEX Equipment for explosive atmospheres   VIEW   VIEW
(EU) 2016/426 GAR Gas appliances   VIEW   VIEW
2014/33/EU LIFT Lifts   VIEW   VIEW
2014/32/EU MID Measuring instruments   VIEW   VIEW
2014/31/EU NAWI Non-automatic weighing instruments   VIEW   VIEW
(EU) 2016/425 PPE Personal protective equipment   VIEW   VIEW
2009/48/EC TOY Toy safety   VIEW   VIEW
2022 Blue Guide   VIEW
Restriction of the use of certain hazardous substances (ROHS)
(EU) 2023/1230
Machinery Regulation (MR)
(EU) 2017/745
Medical devices Regulation (MDR)
Medical devices (MDD)
Active implantable medical devices (AIMDD)
(EU) 2017/746
In vitro diagnostic medical devices Regulation (IVDR)
In vitro diagnostic medical devices (IVDD)
Simple pressure vessels (SPVD)
(EU) 2019/945
Unmanned aircraft systems (UAD)
Recreational Craft (RC)
(EU) 2016/426
Gas appliances (GAR)
Measuring instruments (MID)
Non-automatic weighing instruments (NAWI)
Blue Guide


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EU Declaration of conformity

The EU declaration of conformity is the written statement and the a single declaration drawn up by the manufacturer to demonstrate the fulfilment of the EU requirements relating to a product bearing the CE marking he has manufactured. The declaration shall be in respect of all Community acts applicable to the product containing all information required for the identification of Community harmonisation legislation to which the declaration relates. Read more...


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