CE Certification

Date：2021/10/25　　Clicks：1777

CERTITEK has considerable experience in compliance with European technical directives and standards. As experts in a wide variety of categories, we evaluate your product and provide the documentation necessary to support your Declaration of Conformity to the appropriate directive(s) and apply the CE Mark to your product.

When a Notified Body is required as part of this process (certain products under some directives), we will help identify/selec one and coordinate 

• testing with them. Some of our areas of expertise are listed below, along with a partial list of related equipment categories. Low Voltage Directive (LVD) - 2006/95/EC

Ø  Information Technology Equipment (ITE)

Ø  Telecommunication Equipment

Ø  Laboratory, Test & Measurement and Control Equipment

Ø  Household Appliances

Ø  Audio/Video Equipment

Ø  Industrial Electronic Equipment

• Machinery Directive – 2006/42/EC

Ø  Risk assessment

Ø  Risk mitigation

Ø  Technical file preparation

• General Medical Device Directive (MDD) - 93/42/EEC

Ø  Any medical device not covered by another directive

Ø  Laser devices

• Radio and Telecommunication Terminal Equipment (R&TTE) - 99/5/EC