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Wireless Communication下拉
- Internet of Things authenticat
- UWB Product Certification
- 5G NR Product Certification
- Receiver Product Certification
- SAR testing
- Base station certification
- Interphone product certificati
- Wireless charging product cert
- WiFi Product Certification
- FM/AM Product Certification
- Bluetooth BQB Product Certific
- Mobile communication product c
- Wireless and communication det
Automotive Electronics下拉
- Automotive Electronic Testing
- EMI Test - Conducted Emissions
- EMI Test - Radiation Emission
- EMI testing - low-frequency ma
- EMI Testing - Transient Conduc
- EMS test - low-frequency magne
- EMS Test - High Current Inject
- EMS Testing - Portable Transmi
- EMS Test - Transient Conducted
- EMS Testing - Electrostatic Di
- EMS testing - radiation anti-i
- Electrical performance testing
Automotive Parts Inspection下拉
- Voltage flicker test - Suzhou
- Electrical Fast Pulse Withstan
- Electromagnetic Radiation Tole
- Conducted Immunity Test (CS) -
- Conducted Interference (CE) -
- Common issues with high and lo
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- Three comprehensive vibration
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- Spoiler Three Comprehensive Vi
- Sunvisor Three Comprehensive V
- Comprehensive vibration test o
- Instrument panel/instrument pa
- Temperature shock/cold and hot
- Vibration testing
- Temperature shock test
- Reliability testing
- Automotive ELV&VOC
Chemical Testing下拉
- Hazardous substance testing
- Testing of toys and baby produ
- Food contact material testing
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- Ecological textile testing
- Consumer Product Testing Servi
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- Automotive ELV&VOC
Reliability testing下拉
- Reliability testing
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- Climate environment testing -
- Climatic environmental testing
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- Climatic environment test - co
- Climatic Environmental Testing
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- Mechanical testing - Vibration
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- Other tests - Voltage withstan
- Other tests - Drum drop test
- Other tests - tensile testing
- Other tests - Drum drop test
- Other tests - Paper tape wear
- Other tests -100 grid test
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- Other tests - pencil hardness
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Contact Us
National 24-hour service hotline
86+13560405821
Group Headquarters
E-mail: Lymay.zhong@lcs-cert.com
Address: Juji Industrial Park, Xueziwei, Ngabian, Shajing Street, Baoan District, Shenzhen Building A 1~2F, Building C 3F
Electronic cigarette detection
Product range:
EU TPD testing services
——The EU TPD Directive on the content of electronic cigarettes is detailed
The EU Tobacco Directive TPD (2014/40/EU) entered into force in May 2014, and the two-year transition period has ended. EU member states will complete and implement the legal procedures related to the new directive in May this year. Controls will be imposed on all new tobacco products entering the EU market. E-cigarette products exported to the EU market must meet the requirements of the TPD directive, otherwise they will be banned, confiscated or returned, which will bring huge losses to electronic manufacturers. Therefore, how to make e-cigarette products comply with the EU TPD directive to avoid losses has become a problem that manufacturers must face. This article provides a detailed explanation of the e-cigarette-related issues in the TPD directive.
1. The main contents of the product electronic notice
1. Manufacturer name and contact information
2. List of ingredients and content of emissions
3. Toxicological data
4. Nicotine dose intake information
5. Product composition and production process description
6. Declaration of product quality and safety responsibility
Second, the requirements of cigarette oil and liquid reservoir
Nicotine-containing vape liquids are placed on the market only in professional fillers and filled containers with a volume of no more than 10 mL, in disposable electrons
In cigarettes or single-use cartridges, the volume of the cartridges or reservoir shall not exceed 2ml.
3. Requirements for nicotine
1. In the vape oil containing nicotine, the nicotine content shall not exceed 20mg/ml;
2. Under normal use conditions, the nicotine release of e-cigarettes should be maintained at a stable level.
IV. Overview of the Registration Process (EU TPD)
1. Registration (ECAS) Website:
https://webgate.ec.europa.eu/cas/eim/external/register.cgi
2. Apply for a Submitter ID
2.1 Fill in the form submitted_egisttatingform_en.
2.2 Submit the form submitted_egisttatingform_en and wait for the assignment of the EU Submitter ID (approximately 10 working days to complete)
3. After the registration is completed, notify the administrator by email, stating that the ID registration is successful, and indicating the ECAS and Submitter ID.
4. After success, log in to the account opening information platform (EU-CEG) to fill in the information, upload the attachment, and select different countries to provide the information separately.
U.S. FDA testing and registration services
On May 2016, 5, the FDA (U.S. Agency for Goods and Drug Administration) issued the final rule, Deeming Regulation. The regulation came into effect on August 10, 2016, including all electronic atomized products in the scope of tobacco products, through this regulation, FDA can legally regulate new tobacco products, including ENDS (Electronic Nicotine Deliver Systems), the regulations make a series of regulations on the production, import, packaging, labeling, advertising, promotion, sale, etc. of new tobacco products. Products containing nicotine, or products that may be used with nicotine, are regulated by FDA, not only for finished ENDS products, but also for parts and assemblies, but not accessories. Therefore, all electronic vaping products, including e-cigarettes, must meet the requirements of the FDA Tobacco Control Act, and manufacturers need to comply with the compliance requirements.
1. Production site registration and product list
1. Registration and product listings are only available to manufacturers whose manufacturing activities take place in the United States;
2. Chinese manufacturers do not need to submit production site registration and product list to the US FDA;
3. Definition of Manufacturing: Any person, including any repackaged or remarker, who produces, manufactures, assembles, processes or packages tobacco products, or imports finished tobacco products in the United States for sale or distribution;
4. Time node;
5. Enterprises that already existed before August 2016, 8, if they continue to engage in the manufacture of ENDS products, must complete the site registration and upload the product list before October 8, 2017, update the list before June 10, 12, and complete the registration for the next year before December 2018, 6;
6. Newly established ENDS product manufacturing enterprises after August 2016, 8 must immediately complete the production site registration and product list submission.
2. Submission of health documents
1. Health documentation broadly includes documentation relating to the health, toxicological, behavioural or physiological effects of current or future tobacco products and their constituents (including smoke components), raw materials, components and additives;
2. It can include analytical test reports, research, etc. of the product, but does not include the research in the published literature that has not been done for a specific product;
3. Timeline: Health documents prepared for products marketed before August 2016, 8 must be submitted to FDA by the following dates:
3.1. Large manufacturers - February 2017, 2
3.2. Small manufacturers - November 2017, 11
4. Submission method: eSubmitter and CTP system
(http://ctpportal.fda.gov/ctpportal/login.jsp)
3. Submission of ingredient list
1. Applicable to all products listed in the United States, not limited to products registered in the United States;
2. Each ingredient must be individually identifiable;
3. The type of ingredients can include single chemical substances and compound procurement ingredients;
4. Time node
4.1. Non-small-scale manufacturers that already existed before August 2016, 8 must submit by November 8, 2018;
4.2. The deadline for small-scale manufacturers is May 2018, 5; (Whether the time has returned)
4.3. New products must be submitted 90 days before the launch of the products
5. Submission method: eSubmitter and CTP system
(https:/ctpporta.fda.gov/ctpportal/login.jsp)
IV. Report of Hazardous and Potentially Hazardous Substances (HPHC)
1. Hazardous and potentially harmful substances means any compound present in ENDS products or their fumes that may cause direct or indirect harm to consumers;
2. Time node:
2.1.November 2019, 11;
2.2. Products listed after November 2019, 11 must be submitted 8 days before listing.
3. Submission method: eSubmitter and CTP system
(https:/ctpporta.fda.gov/ctpportal/login.jsp)
V. Market Access Application (PMTA)
1. Electronic cigarettes listed before August 2016, 8 must submit PMTA before August 8, 2022;
2. Must demonstrate that the product is suitable for protecting public health;
3. Submit scientific research and analysis related to products
3.1. Product analysis;
3.1.2. Product performance, such as dimensions, overall structure description, features involved, etc.;
3.1.3. Description of the principle of operation, completeness of the consumer's mode of use;
3.1.4. Description of the whole process of product production;
3.2. Components, ingredients, additives;
3.2. Health research;
3.2.1. Clinical research;
3.2.2. Consumer perception data;
3.2.3. Usage Data;
3.2.4. Human factors;
3.2.5. Non-clinical research on abuse of liability;
3.2.6. Review of scientific literature.
6. Services we may provide
Luxshare Testing is one of the earliest independent third-party testing institutions in China to conduct electronic cigarette testing, with a strong technical research and development team equipped with advanced testing instruments. Maintain a good cooperative relationship with the world's most influential e-cigarette brands. Our detection methods for electronic cigarette oil and smoke have been recognized by the China National Accreditation Service for Conformity Assessment (CNAS), and the reports issued have been widely recognized and praised internationally.
Our company can provide customers with the following testing services:
1. Assist in the registration of production site and product list;
2. Healthy and stable production and submission
3. Ingredient list registration
4. Hazardous and Potentially Hazardous Substances (HPHC) testing and report submission;
5. Assistance with Market Access Applications (PMTA).
E-cigarette UAE certification
1. What is ECAS certification?
The UAE Standards Authority (ESMA) was established under UAE Federal Law (2001) of 28 and is the only national standards body and certification body in the UAE. In order to effectively implement the UAE national standards, ESMA's Conformity Assessment Department has implemented a product safety certification system, referred to as the Emirates Conformity Assessment Scheme (ECAS), which has been implemented since June 28, 2001. According to the ECAS program requirements, all regulated products must apply for and obtain a COC Certificate of Conformity as a customs clearance and sales pass. ECAS certification not only includes safety, but also covers the safety testing, performance testing, functional inspection, hazardous substance testing and other possible aspects of electronic and electrical appliances.
2. ECAS registration framework
1. ECAS registration of e-cigarette devices
2. ECAS registration of e-cigarette labels
3. ECAS registration of electronic cigarette RoHS
4. Other information, test reports, etc
5. Get the ECAS Registration Certificate (COC) of the e-cigarette
3. ECAS registration process
1. Register an account on the ESMA website
2. Submit an application for a Certificate of Conformity
3. Upload the required documents
4. Payment
5. Document review
6. If the product fully meets all the requirements, the system will notify the customer
7. Obtain a Certificate of Conformity (COC Certificate)
4. ECAS registration fees
Label ECAS registration (fee 6100AED)
RoHS ECAS registration (fee 4300AED)
ECAS registration for e-cigarette devices (fee 6100AED)
ECAS registration for e-cigarette liquid/cartridges (fee 6100AED)
Other tests for e-cigarettes
1. Battery test items
1. The battery applies for CB certification, and the standard is IEC62133.
2. The battery applies for IEC report, and the standard is IEC62133 or IEC60086.
2. Safety test items
1. Plug test report, the standard is electrical safety part 60335-1
2. Electronic cigarette safety standard, UL8139-2017
3. Quality inspection report
Third, EMC test items
1. CE certification
2. FCC certification
4. Chemical test items
1. RoHS test report, with ISO 17025 qualification
2. TPD emission test report
3. Additive component content test report
4. Emission composition test for e-cigarette emissions
5. E-cigarette emission (Emission) TPM test
6. Electronic cigarette oil composition analysis test
7. Electronic cigarette oil nicotine content test
8. Electronic cigarette oil PG&VG content test
9. E-cigarette EU registration consulting services
10. Electronic cigarette food contact material (FCM) test
11. Electronic cigarette finished products, EU RoHS REACH and other regulations testing
30
individual
Large-scale experimental base
150
individual
Professional Lab
30
All kinds of
Analysis Method
2700
million times
Testing/year
Contact Us
National 24-hour service hotline
Juji Industrial Park, Xueziwei, Ngabian, Shajing Street, Baoan District, Shenzhen Building A 1~2F, Building C 3F
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Address：Juji Industrial Park, Xueziwei, Ngabian, Shajing Street, Baoan District, Shenzhen Building A 1~2F, Building C 3F mobile：86+13560405821 Mailbox：Lymay.zhong@lcs-cert.com
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