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Wi-Fi Certification
In the modern world, everyone needs a reliable and fast Wi-Fi connection. No serious business or individual can do without the fast and secure Internet. Therefore, Wi-Fi certification is a special seal of approval recognized worldwide. That is why developers of all types of wireless devices, which are sold worldwide, need valid Wi-Fi certificates. Such a certificate will guarantee that their products are of the highest quality and can provide flawless connection. In this publication, you will learn about Wi-Fi testing in detail.
What Is Wi-Fi Certification?
Currently, Wi-Fi devices are tremendously popular worldwide. People use many electronic products that need a stable Wi-Fi connection to perform their functions every day. You might have already noticed that many devices have the Wi-Fi Certified logo on the packaging. To get the Wi-Fi logo, the developers of wireless devices must obtain an official Wi-Fi certification from the Wi-Fi Alliance.
Wi-Fi certificates are used for security purposes. When computers, phones, and apps have such a certificate, it confirms that they can access certain data or functions. Generally, Wi-Fi Certified is the mark of approval for all wireless products. It is recognized worldwide and indicates that products comply with industry standards for interoperability, security, and application-specific protocols. After the product passes testing, the supplier or manufacturer obtains the right to use the Wi-Fi Certified official logo.
Plenty of business products are subject to the certification. Among them are smartphones, home appliances, computers, consumer electronics, and many more. The Wifi Alliance provides its customers with effective tools for FlexTrack and QuickTrack certification processes. They can help the company’s clients confirm the reliability of their products. Moreover, clients can integrate these tools in developing their products and, therefore, guarantee their highest quality.
Wi-Fi Testing Process
The key certification processes are:
- FlexTrack. FlexTrack provides a flexible Wi-Fi functionality customization that is built into components.
- QuickTrack. This certification path provides lower costs to get your product Wi-Fi Certified. Hence, members can build various products based on Qualified Solutions. These are chipsets, modules, and some other solutions, which are tested watchfully.
As a rule, the Alliance certification consists of three types of tests. Hence, your new product will be tested for the following:
- Compatibility. It is the most important test for getting the Wi-Fi Certified label. It means that your new wireless device should be well-matched with certified devices from other vendors.
- Conformity. Your new wireless equipment should conform to specific elements of the IEEE 802.11 standard.
- Performance. Your product should meet the minimum performance requirements.
Why Do You Need Wi-Fi Testing?
With the increased range and variety of Wi-Fi products in the industry – from entry points to IoT frameworks – it is now more vital than ever to provide customized testing choices that guarantee the best quality Wi-Fi. According to the Wi-Fi Alliance’s press statement, Wi-Fi certified products are chipsets or modules that satisfy industry-agreed Wi-Fi qualifying criteria.
The Wi-Fi Alliance claims that the certification choice allows for testing at a Wi-Fi Alliance member’s home facility or, as is customary, at a Wi-Fi Alliance-authorized lab (ATL). According to the Wi-Fi Alliance, the new approach cuts expenses and shortens the time required to complete certification verification. The new method could reduce the time for Wi-Fi-certified devices created by the Wi-Fi Alliance’s members in the long run.
360Compliance will comply with Wi-Fi Alliance testing requirements, demonstrating your wireless device’s capacity to communicate with other authorized gadgets in a Wi-Fi network.
How To Get The Wi-Fi Certification?
To get the Wi-Fi certification, a company must perform the following steps:
- The company must be a member of the Wi-Fi Alliance. The annual membership cost as of 2023 is $5,150.
- The Wi-Fi Alliance lab tests all Wi-Fi products. It usually takes up to four weeks to pass all the necessary tests for the certification.
- Once certified, the company can use the Wi-Fi Certification logo and certification marks.
Advantages Of Getting The Wi-Fi Certification
The Wi-Fi Alliance certification has plenty of benefits for businesses. Let us enumerate the key ones.
- Increased standards of security.
- Customers trust only fully certified products.
- Certified products will help to grow your business profits significantly.
- Greater satisfaction of your customers and higher sales.
- Certification decreases support costs significantly.
- It ensures compatibility with other equipment manufacturers’ products.
- Certification speeds up the process of your product development.
- The Wi-Fi Certified seal guarantees the recognition of your product worldwide and helps it enter new markets more quickly.
Wi-Fi Alliance Standards
The Wi-Fi Alliance is an organization that is considered to be the owner of the Wi-Fi trademark. Wireless technology producers should use it to brand their devices certified for Wi-Fi compatibility. The organization started to work in 1999, with its headquarters in Austin, Texas.
The organization mostly deals with Wi-Fi certification. According to the Wi-Fi Alliance testing standards, your wireless gadget must be compatible with other certified devices in the same WLAN. You should remember that you don’t necessarily need to get the Wi-Fi Certified label.
However, getting one will attract more clients to your product as they know that such a label means the 100% reliability of a wireless device.
Get The Wi-Fi Certification With 360Compliance
Now, you know what Wi-Fi certification is and its benefits for businesses and individuals. So, if your products have the Wi-Fi-certified label, it guarantees that your Wi-Fi devices are trusted, reliable, and secure. You can get this certification with 360Compliance. To order this service, provide us with the following info:
- Company name.
- Your name, email, and phone number.
- Choose a certificate type and press the Send button.
Contact 360Compliance today to discuss the certification details.
Other Certifications
CE Certification
Why is CE Certification Important? CE certification confirms that the product entered the market legally, has all the permits, and does not pose any threat to human health or the safety and integrity of the environment. Thus, the CE mark signals both buyers and official regulators about the successful completion of all testing and certifying procedures. What Countries Require CE Marking? The mandatory CE certification applies to products entering the market of all 30 countries of the European Economic Area (EEA). It also covers Switzerland and Turkey, the United Kingdom, which have signed a number of bilateral agreements with the EU, including the CE marking requirement. Additionally, the UK indefinitely recognizes the EU's CE mark for various manufactured goods placed on the UK market. What Products Need a CE Certification? To determine whether a product requires CE Certification, manufacturers should consult the relevant EU directives and harmonized standards. Notified bodies, independent organizations authorized to assess product compliance with EU directives, can also provide guidance. Product Category Examples Electrical equipment Household appliances, power tools, lighting, cables Toys Dolls, action figures, toy cars, construction sets Machinery Industrial machinery, agricultural machinery, construction machinery Medical devices Surgical instruments, implants, diagnostic equipment Construction products Cement, steel, windows, doors Personal protective equipment Safety helmets, goggles, gloves, boots Pressure equipment Gas cylinders, boilers, pressure cookers Gas appliances Cookers, heaters, gas water heaters Aerosols Spray paint, deodorants, insecticides Telecommunications equipment Mobile phones, routers, modems Radio equipment Radios, televisions, Bluetooth devices Lifts Escalators, elevators, dumbwaiters Explosive devices Fireworks, detonators, ammunition What Products Do Not Require a CE Marking? Not all products imported into the listed countries require CE marking certification. In particular, goods belonging to the following categories, which are covered by other Directives, are subject to a different type of certification: Chemical products Cosmetics Food products Pharmaceuticals How to Obtain CE Certification? Obtaining a CE certificate involves a systematic process: Identify Applicable Directives The Directives include general safety requirements for products placed on the market. The specific parameters and technical requirements are detailed in the harmonized standards. If a product does not fall under any Directives requiring CE marking, it must still comply with a document outlining general safety requirements. Directive Number Product Category 2014/35/EU Low Voltage Directive (LVD) 2014/30/EU Electromagnetic Compatibility (EMC) 2011/65/EU Restriction of Hazardous Substances (RoHS) 2014/53/EU Radio Equipment 2014/34/EU Equipment and Protective Systems for Use in Explosive Atmospheres (ATEX) Regulation (EU) 2017/745 Medical Devices Regulation (EU) No 305/2011 Construction Products 2006/42/EC Machinery Regulation (EU) 2016/425 Personal Protective Equipment 2014/31/EU Non-automatic Weighing Instruments Regulation (EU) 2016/426 Appliances Burning Gaseous Fuels 2014/28/EU Explosives for Civil Uses 90/385/EEC Active Implantable Medical Devices 98/79/EC In Vitro Diagnostic Medical Devices 2014/90/EU Marine Equipment Directive 2013/53/EU Recreational Craft 2014/33/EU Lifts 2014/68/EU Pressure Equipment Regulation (EU) 2016/424 Cableway Installations to Carry Persons 2014/32/EU Measuring Instruments 2013/29/EU Pyrotechnic Articles Full list of CE directives you can find here Identify the requirements for the product Each Directive specifies essential requirements that a product must meet. To demonstrate conformity, manufacturers must identify applicable 'harmonized European Norms' (hENs), which are standards that offer a presumption of conformity to the essential requirements. These standards vary depending on the product's classification and intended use. Harmonized standards, available on the European Commission’s website, simplify compliance through clear frameworks. Determine if third-party assessment is needed Certain directives may require third-party assessment by a Notified Body (NB), an organization authorized by European authorities. For example, the Medical Devices directive and others mandate the use of an NB. However, the EU has reduced the number of products requiring NB assessment, placing more responsibility on manufacturers. Assess Product Conformity Conduct a thorough assessment of your product to ensure it conforms to the essential requirements outlined in the relevant directives. This step may involve testing and verification processes to demonstrate that your product meets the necessary safety and environmental standards. Compile a Technical File Create a comprehensive technical file that documents every aspect of your product's design, development, and manufacturing process. This technical file, also known as the Technical Construction File, should include technical descriptions, drawings, circuit diagrams, bills of materials, specifications, test reports, and other relevant information. The file serves as evidence of conformity and must be maintained for up to 10 years after the last unit is manufactured. Make a Declaration And Affix The CE Mark When satisfied that the product conforms to the applicable CE Marking Directives, the manufacturer must complete a Declaration of Conformity. It includes information about the product, directives, standards applied, and the responsible party in the company. Following this, affix the CE mark visibly on the product, signaling compliance with EU standards. This is the final stage, after which the product may be launched to the EU and EEA markets. Responsibility of Manufacturers for CE Certification To complete the standard procedure for obtaining the CE mark, manufacturers must find out which EU Directive regulates the access of products of their category to the market and check compliance with all regulations. After that, a conformity assessment is carried out, based on which a technical file is prepared. Further, the EU-authorized body examines the documents, and the manufacturer issues the EC Declaration of Conformity (DoC). When all documents are certified and the CE mark is received, the manufacturer can label with this mark their products and packaging. Responsibility of Distributors for Products with a CE Mark Distributors of goods in the EU market must ensure that the CE conformity mark has not yet expired and that the certificate itself is not fake. They also check the placement of the stamp on the product or its packaging since marking is the responsibility of the manufacturer. What Are the Benefits of CE Certification? There are several advantages to CE certification, including: Free movement of goods within the EEA Allows manufacturers to freely circulate their products within the EEA without facing additional technical barriers to trade. Increased market access CE certification can help manufacturers gain access to new markets in the EEA, as well as in other countries that recognize the EC marking. Enhanced product safety Helps to ensure that products meet high standards of safety and environmental protection. Improved consumer confidence CE certification indicates independent compliance with EU safety requirements, boosting consumer confidence. Become CE Certified with 360Compliance The CE marking procedure can be tedious and incomprehensible to non-professionals. However, the 360Compliance team will help you pass all stages of certification quickly, competently, and successfully. You will receive full project management with no hassle. You are also guaranteed technical support and a transparent pricing policy. To start the testing & certification process for obtaining a CE stamp, contact the 360Compliance team in any convenient way and get all the answers and instantly initiate the certification procedure. Frequently Asked Questions About CE Marking For How Long is a CE Certificate Valid? For each product group, a certain validity period is established, but in most cases, it is 3 years. After that, you need to go through the re-certification procedure. However, there are products for which the CE label is valid for 10 years or more. What are the Penalties for the Absence of a CE Compliance Certificate? Punishment for selling goods without the certificates in countries where the CE marking is mandatory varies widely from administrative to criminal liability. The specific article of the law that will be applied depends on the damage that a given product can cause to people or the environment. How to Get a CE Certificate? To obtain the CE stamp, it is necessary to go through a risk assessment procedure for the products offered. For this, you need to study the standards of the specific Directive that regulates access to the market for this type of products, make up a technical file, and pass testing. When all permits are issued, CE marking can be applied to the offered products. How to Authenticate a CE Certificate? You can authenticate a CE label using the official database. Also, it is possible to contact the official authority that issued the certificate and request details on this product. If it turns out that this product is not registered with official institutions, you are dealing with fake certification.
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EMC Directive 2014/30/EU
Do you manufacture or sell electrical or electronic equipment in the European Union (EU)? If so, you'll need to ensure your products comply with the Electromagnetic Compatibility (EMC) Directive 2014/30/EU. Wondering how you can streamline the compliance process to ensure your products meet the EU's stringent electromagnetic compatibility requirements? 360 Compliance is here to guide you through every step, ensuring your products not only comply but thrive in the European market. What is CE EMC Certification? CE EMC Certification is a mark that indicates a product's compliance with Electromagnetic Compatibility (EMC) requirements in the European Union. EMC is crucial because electronic devices emit electromagnetic waves during operation, and without proper EMC measures, these emissions can lead to Electromagnetic Interference (EMI). The CE mark, which stands for Conformité Européenne, is a mandatory certification for products sold within the European Economic Area (EEA). It signifies that a product meets the essential EMC standards set by the European Union to ensure that it won't cause or be susceptible to electromagnetic interference. This interference could affect the proper functioning of other nearby electronic devices. The certification process is guided by Directive 2014/30/EU, which outlines the specific EMC requirements that products must meet to obtain the CE mark. This directive establishes the legal framework for electromagnetic compatibility and mandates that manufacturers thoroughly test their products for compliance. The goal is to guarantee that electronic devices can coexist harmoniously in the European market without causing disruption or compromise in functionality. Which Products Need the CE EMC Mark? If your product falls into the category of devices that can emit electromagnetic waves during operation, it likely requires the CE EMC mark. Here are some examples of products that typically need this certification: Electrical Appliances: Household appliances such as washing machines, refrigerators, and microwave. Information Technology Equipment: Computers, laptops, servers, and networking equipment. Consumer Electronics: This includes a broad range of devices like televisions, audio equipment, and gaming consoles. Medical Devices: Equipment used in the medical field, such as diagnostic machines and monitoring devices. Telecommunications Equipment: Phones, routers, and other communication devices. Industrial Machinery: Various types of machinery used in industrial settings, like manufacturing equipment and automation systems. Lighting Products: From simple light bulbs to complex lighting systems. Electronic Toys: Children's toys that incorporate electronic components or emit electromagnetic signals during play. Why is EMC Directive Important? Ensuring Market Access: Legal Compliance: CE EMC Certification is a legal requirement for placing products in the EU market. Non-compliance can result in serious consequences, including fines and withdrawal of products from the market. Enhanced Market Credibility: Products with CE EMC Certification signal adherence to high-quality standards, enhancing your brand's credibility and customer trust. Quality Assurance: Product Reliability: EMC Certification ensures that your products can function in the presence of electromagnetic disturbances, making them more reliable. Reduced Interference: Certification reduces the risk of your products causing interference with other electronic devices, preventing potential issues for end-users. How to Get CE EMC Certification? Step-by-Step Guidance: Consultation: Initiate the process with a consultation to understand your product and specific certification needs. Pre-assessment: Identify potential EMC issues and address them before formal testing to expedite the certification process. Testing and Evaluation: Utilize our accredited laboratories for comprehensive emissions and immunity testing. Documentation Support: Our team assists in preparing the necessary technical documentation required for certification. Declaration of Conformity: Once certified, we help you issue the Declaration of Conformity and affix the CE mark to your product. How long will testing take? The EMC CE certification procedure takes 4 to 6 weeks on average. If the product belongs to an industry that is regulated by other directives (e.g. CE RED), it is subject to additional tests, which increases the time required. Manufacturer's Responsibilities Related to EMC CE Certification The company that develops a product shall design it according to EMC CE norms and confirm compliance with the norms by independent laboratory tests. It is also required to: indicate the actual electromagnetic radiation level in the documentation; warn about the possible hazards associated with the use of the device; provide the user with operating instructions; indicate geographical restrictions on the use of the product, if any; keep a register of complaints; store certificates and declarations of conformity for at least 10 years; cooperate with local authorities and provide product samples to the authorities. Quick and Easy EMC CE Certification with 360Compliance Obtaining CE EMC Certification is not just a regulatory obligation; it is a strategic move to ensure your products' quality, compliance, and market competitiveness. By investing in certification, your business can access new markets, build trust with customers, and stay ahead in the dynamic world of electronics. At 360Compliance, we simplify the process, offering expert guidance and tailored solutions to ensure your products meet the highest standards of electromagnetic compatibility. Contact us to get transparent pricing, clear timelines, and technical support at all stages of the procedure.
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CE Mark Medical Device
Do you manufacture or plan to sell medical devices in the European Union (EU)? If so, obtaining CE marking for medical devices is essential for legal market access. This signifies compliance with the Medical Devices Regulation (MDR) 2017/745. Looking for a partner to demystify the CE marking process and ensure your medical devices comply with EU regulations? At 360Compliance, we're here to provide guidance and support to address any questions you may have. What is CE MD Certification? CE MD certification is a mandatory requirement for all medical devices that are sold in the European Union. The CE mark is a symbol that indicates that a product has met all of the applicable EU directives and regulations. To obtain CE marking for medical devices, manufacturers must adhere to the regulatory framework outlined in the Medical Devices Regulation (MDR) or the In Vitro Diagnostic Regulation (IVDR). The primary objective of CE approval for medical devices is to ensure the safety, effectiveness, and alignment with the needs of patients and healthcare professionals. The process is regulated by EU Directive 2017/745 and relevant industry regulations, including 90/385/EEC, 93/42/EEC, 98/79/EC, and 722/2012. Which Products Require MDR CE Marking? CE MD marking is mandatory for a wide range of medical devices, including but not limited to: Diagnostic Equipment; Implants; Surgical Instruments; Monitoring Devices; Dental Products; Rehabilitation Equipment. Manufacturers must ensure their products align with specific classifications and requirements outlined in the applicable directives. Which products do not need the CE mark medical device? CE medical device certification is unnecessary if the product does not meet the definition of a medical device outlined in EU Directive 2017/745 (MDR). In that case, other industry regulations, like those governing radio frequency or electromagnetic radiation, are applicable. Additionally, products can be sold without a CE certificate if alternative standards have been set for them, as seen with medicines, food products, cosmetics, and chemicals. CE Certification Process for Medical Devices The CE certification process for medical devices involves several key steps: Legal Requirement CE marking is mandatory for medical devices under the EU Medical Devices Regulation (MDR) or the In Vitro Diagnostic Medical Devices Regulation (IVDR), depending on the nature of the product. Conformity Assessment To obtain CE marking, manufacturers must undergo a conformity assessment, which involves demonstrating that the medical device complies with the relevant essential requirements and standards. Particularly the IEC 60601 series, which specifically addresses the safety and essential performance of medical electrical equipment. Classification of Devices Classifying devices involves categorizing medical devices into different classes based on their risk level. The classification determines the conformity assessment procedure that the manufacturer must follow. Technical Documentation Manufacturers must create and maintain technical documentation supporting the conformity of the medical device. This documentation should cover aspects such as design, manufacturing, risk assessment, and labeling. Notified Bodies In many cases, a Notified Body, an independent third-party organization, is involved in the conformity assessment process. The Notified Body assesses the technical documentation and issues a certificate if the requirements are met. Post-Market Surveillance CE marking is not a one-time event. Manufacturers must continue to monitor their products after they enter the market. Post-market surveillance involves tracking the device's performance, addressing any safety concerns, and updating documentation as needed. Unique Device Identification (UDI) The EU MDR and IVDR require the use of a Unique Device Identification system, allowing for traceability and improved post-market surveillance. The timeframe for issuing the certificate varies depending on the niche and the application of the device. The average time for a Class A device is 4 to 8 weeks. Clinical testing of Class B and C devices can take several months. Benefits of CE Certification for Medical Devices Market Access Achieving CE certification opens the doors to the vast European market, allowing manufacturers to distribute and sell their medical devices within the EU. Compliance with Regulations CE certification ensures that your medical device complies with the stringent regulations and standards set by the European authorities, fostering trust among healthcare professionals and end-users. Enhanced Reputation Displaying the CE mark on your medical devices demonstrates a commitment to quality and safety, enhancing your brand's reputation in the competitive healthcare industry. Risk Mitigation Compliance with CE mark medical device requirements helps mitigate legal and financial risks associated with non-compliance, ensuring that your products meet the highest safety and performance standards. Why Choose 360Compliance For CE Approval For Medical Devices? We provide a full range of CE certification services for medical devices. Our employees provide assistance with all the stages of this procedure from evaluating the legal environment and determining the class of equipment to the paperwork and cooperation with authorized bodies. We guarantee transparent prices, clear deadlines, and convenient technical support. Get your certificate quickly and with a minimum of effort by leaving an application on our website to learn more about our services!
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