EU (European) Directive Testing
F2 Labs has more than 20 years of experience in assisting our clients with European product compliance evaluation and testing to the applicable EN standards under the EU Directives so that they can obtain the CE mark for their product(s). Products must adhere to the appropriate EU Directives in order for CE compliance and to be sold on the European market.
We offer a number of EU Directive evaluation and testing services to ensure your product meets the legal requirements for European certification and compliance.
F2 Labs provides expert evaluation, testing, and (where required) Notified Body services for the following EU Directives:
- Radio Equipment Directive 2014/53/EU (RED), formerly R&TTE Directive
- Electromagnetic Compatibility (EMC) Directive 2014/30/EU
- Equipment for Explosive Atmospheres (ATEX) Directive 2014/34/EU
- General Product Safety Directive 2001/95/EC
- Low Voltage Directive 2014/35/EU
- Machinery Directive 2006/42/EC
- Medical Device Directive 93/42/EEC
Contact us today to learn more about how F2 Labs can help your organization with how to get CE certification. We can help you whether you are ready to ship or in the bid phase of your project.
Frequently Asked Questions
What is EU Directive Testing?
EU Directive Testing involves evaluating and testing products to ensure they comply with the specific EN standards required by the European Union Directives. This process is crucial for obtaining the CE mark, allowing products to be sold on the European market.
Why is CE Certification Important?
CE certification signifies that a product has met EU safety, health, and environmental protection requirements. It is a mandatory conformity mark for products placed on the market in the European Economic Area (EEA), facilitating free movement and sale within the EEA.
What EU Directives Does F2 Labs Cover?
F2 Labs provides testing and evaluation for a range of EU Directives, including the Radio Equipment Directive (RED), Electromagnetic Compatibility (EMC) Directive, ATEX Directive for explosive atmospheres, Low Voltage Directive, Machinery Directive, and the Medical Device Regulation.
How Can F2 Labs Assist with EU Directive Compliance?
F2 Labs offers expert evaluation, testing services to ensure products meet the legal requirements for European certification and compliance. They assist clients in navigating the complex process of obtaining CE certification.
What Types of Products Require EU Directive Testing?
A wide range of products, including radio and telecommunications equipment, electrical devices, machinery, medical devices, and products intended for use in potentially explosive atmospheres, require EU Directive Testing to ensure they meet specific regulatory standards for safety and performance.
Can F2 Labs Provide Notified Body Services?
Yes, F2 Labs provides Notified Body services for certain directives where such services are required. A Notified Body is an organization designated by an EU country to assess the conformity of certain products before being placed on the market.
How Long Has F2 Labs Been Assisting with European Product Compliance?
F2 Labs has over 25 years of experience in assisting clients with European product compliance, evaluation, and testing. Their extensive experience ensures that clients receive knowledgeable and efficient service to achieve CE certification.
How to Start the Process of EU Directive Compliance Testing with F2 Labs?
To start the process of EU Directive compliance testing, you can contact F2 Labs directly by clicking here. They can assist whether your product is ready to ship or still in the bid phase of your project, offering guidance on the specific requirements and steps needed for CE certification.
