WWW. CE-Mark.com Site Map

CE Marking Information:

• Exporting to Europe and CE Marking
• European Countries that Require CE Marking
• European Union Directives
• CE Marking Enforcement

European Union Directives:

• ATEX- Equipment For Explosive Atmospheres 94/9/EC
• ATEX - Effective April 2016 2014/34/EU
• Batteries2006/66/EC
• Decision on the Marketing of Products 768/2008/EC
• Electromagnetic Compatibility (EMC) 2004/108/EC
• General Product Safety 2001/95/EC
• In-Vitro Diagnostic Devices Regulation (EU) 2017/746
• Low Voltage 2006/95/EC
• Machinery2006/42/EC
• Medical Devices Regulation (EU) 2017/745
• Personal Protective Equipmenr 89686/EEC
• Phthalates 2005/84/EC
• Pressure Equipment 97/23/EC
• Radio Equipment2014/53/EU
• Regulation on Market Surveillance 765/2008
• RoHS2 - Restriction on the use of certain hazardous substances in electrical and electronic equipment 2011/65/EU
• WEEE-Waste Electrical and Electronic Equipment 2012/19/EU
• UK Machinery Regulations

CE Marking Medical Devices:

• CE Mark Medical devices Technical File
• What Manufacturers Need to Know and Do

CE Marking In-Vitro Diagnostic Medical Devices:

• Self-Certification of IVDD

CE Marking Personal Protective Equipment:

• Is it Personal Protctive Equipment or a Medical Device?
• European Authorized representative for Personal Protective Equipment
• FAQ of the role of the Authorized Representative

CE Marking Machinery

• CE Marking and What Manufacturers Need to Know and Do
• Self Certification of your machinery
• Technical File Required for all machinery
• QNET's Advisory technical file writing service
• CE Marking Pumps
• QNET's CE design engineering solutions
• EU Machinery translation requirements
• RoHS Directive- What Manufacturers Need to Know and Do
• EU Authorized representative For Machinery proposal request
• FAQ about the role of the Authorized Representative

ATEX - Equipment used in explosive atmospheres:

• ATEX Requirements in the European Union

Pressure Equipment

• Pressure Equipment in the EU requirements

FDA

• FDA 510(k) prepared by QNET

EU Authorized Representative

• Medical Device Authorized Representative
• Machinery Authorized Representative
• Personal Protective Authorized Representative
• Request For Medical Device Authorized Representative
• Request for Machinery Authorized Representative