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CQC-C0801-2014: China Compulsory Certification Implementation Detailed-Rules - Audio and video equipment
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China Compulsory Certification Implementation Detailed-Rules - Audio and video equipment
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CQC-C0801-2014
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PDF similar to CQC-C0801-2014
Standard similar to CQC-C0801-2014 CQC-C0901 CQC-C0701 BJS 201706 CQC-C0302 Basic data | Standard ID | CQC-C0801-2014 (CQC C0801-2014; CQC-C08-01-2014; CQC-C0801-2014) | | Description (Translated English) | China Compulsory Certification Implementation Detailed-Rules - Audio and video equipment | | Sector / Industry | China Quality Certification Center - CCC Implementation Detailed-Rules | | Classification of Chinese Standard | CQC | | Word Count Estimation | 25,216 | | Date of Issue | 7/16/2014 | | Date of Implementation | 9/1/2014 | | Older Standard (superseded by this standard) | CQC-01C-017-2010 | | Regulation (derived from) | Notice No. 23 of the State Certification and Accreditation Administration, No. 23 of the State Certification and Accreditation Administration | | Issuing agency(ies) | China Quality Certification Center | | Summary | This document specifies the China Compulsory Certification (CCC) implementation Detailed-Rules for Audio and video equipment. This document defines the Audio and video equipment's certification unit; certification entrusting; document requirements; sample | CQC-C0801-2014: China Compulsory Certification Implementation Detailed-Rules - Audio and video equipment
---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
China Compulsory Certification Implementation Detailed-Rules-Audio and video equipment
Scope of application
The audio and video equipment implementation rules (hereinafter referred to as the implementation rules) are based on the "compulsory product certification
Implementation Rules for Audio and Video Equipment (CNCA-C08-01..2014) (hereinafter referred to as the Implementation Rules)
It is required to prepare and use it as a supporting document for the implementation rules of certification.
The content of the product scope, certification basis, etc. and the implementation rules applicable to this implementation details include
Relevant regulations are consistent, and according to the National Certification and Accreditation Regulatory Commission (hereinafter referred to as the national certification
Supervisory Committee)
The announcement of catalogue definition and catalogue adjustment will be adjusted.
CQC, in accordance with the provisions of the certification implementation rules, is committed to maintaining the effectiveness of product certification and improving product quality.
To formulate and publish the implementation details of this certification.
Establish the classification management requirements of production enterprises, and combine the classification of production enterprises to clarify the production of audio and video equipment.
Implementation requirements for certification. PP
2. Certification standards
Implementation in accordance with Article 2 of the Implementation Rules.
3. Authentication mode
The audio and video equipment can choose from the following authentication modes.
Mode 1.
Class I or II equipment. supervision after type test
Equipment other than Category I or II. Follow-up inspection after type test
The above-mentioned post-certification supervision refers to follow-up inspection after certification, sampling at the production site for testing, or
Inspection, market sampling or inspection.
Mode 2.
Supervision after type test
The above-mentioned post-certification supervision refers to follow-up inspection after certification, sampling at the production site for testing, or
One or a combination of inspection, market sampling or inspection.
Type A and B manufacturing companies can adopt the mode 1 for certification.
Type C and D production enterprises should adopt Model 2 for certification.
Mode 3.
Supervision after initial inspection of type test
The above-mentioned post-certification supervision refers to follow-up inspection after certification, sampling at the production site for testing, or
One or a combination of inspection, market sampling or inspection.
In order to avoid the risk of non-compliance of products placed on the market, Class A, B, C, and D production
Companies can also voluntarily choose Model 3 for certification.
4. Division of authentication unit
In accordance with Article 4 of the Implementation Rules.
5. Authentication commission
5.1. Application for and acceptance of certification
The certification client submits a certification commission to CQC through the network. Certification Committee
The trustee must fill in the necessary company information and product information as required, and provide business registration if necessary
Certificate, organization code, electrical schematic diagram, agreement, etc.
CQC reviews applications in accordance with relevant requirements, and issues acceptance or rejection within 2 working days
Notice, or require the certification client to re-apply for certification after rectification.
5.2. Application Information
The certification client shall provide relevant application materials to the CQC and/or laboratory as required by the certification scheme
And technical materials, including but not limited to.
(1) Application for certification;
(2) Registration certificate of certification client, producer, and manufacturing enterprise (such as business license, organization
Institution code certificate, etc.) (if necessary);
(3) Self-assessment report/declaration of the factory's factory quality assurance capability (if necessary)
(4) Factory inspection questionnaire (if necessary);
(5) Relevant agreements or contracts signed between certification clients, producers, and production enterprises (such as
0DM agreement, OEM agreement, authorization letter, etc.) (if necessary);
(6) Product description information, mainly including. model description, technical parameters, key components and
6.1.
/ Or bill of materials, electrical schematics, differences in products of different specifications included in the same certification unit
Instructions, etc. (if necessary);
(7) Chinese instruction manual, Chinese nameplate and warning signs (if necessary);
(8) Materials such as the appointment letter of the person in charge of certification technology and the CQC assessment certification (if any);
(9) For the application for change, the supporting documents of the relevant change items (such as the enterprise name change, administrative area
Domain redistribution, etc.) (if necessary);
(1 0) Other required documents.
5.3. Implementation arrangements
After accepting the certification application, the CQC shall comply with the classification management requirements of the manufacturing enterprise and the relevant requirements submitted by the enterprise.
Product information, etc., formulate the certification scheme, and notify the certification client. Certification schemes usually include the following.
(1) List of application materials to be submitted;
(2) Requirements for sample submission for type test;
(3) laboratory information;
(4) The required certification process and time limit;
(5) Estimated certification costs;
(6) Contact information of CQC staff;
(7) Other matters that need to be explained.
6. Certification implementation
Type test
6.1.1. Type test plan
The content of the type test plan includes the requirements for type test samples (see 6.1.2 of these Rules), test targets
Quasi-projects (see 6.1.3 of these Rules) and laboratory information.
6.12 Requirements for type test samples
Under normal circumstances, the representative of the test is selected by the certification client according to the requirements of CQC.
Used for detection.
The products of the same manufacturer, the same product category, and different production enterprises should be divided into different applications
The unit and type test are only performed on the samples of one manufacturer. When necessary, other manufacturers shall
Provide samples and related information for verification by the certification body.
If there is only one model in the application unit, the sample is selected for this model.
When applying a series of products for the same application unit, the sample should be selected from the series of products.
Representative models, and the samples selected should cover the safety requirements and electrical requirements of the series of products as much as possible.
Magnetic compatibility requirements, if it cannot be covered, other model samples in the application unit should be selected to supplement the difference
Foreign test.
The number of representative model samples of the application unit is 2 (eg 1 CB sample is approved). Correct
Power adapter (including charger/discharger) can supply the highest output voltage and output power according to the characteristics of the series products
The model with the highest flow.
The number of supplementary test samples depends on the representative model samples and covers the safety requirements of the products in the application unit.
Depending on the actual situation of electromagnetic compatibility requirements, representative model samples and supplementary test samples
Under the premise of the safety requirements and electromagnetic compatibility requirements of the series of products in the cover application unit, it should be reduced as much as possible
Number of supplementary test samples and supplementary test items o
The requirements for the list of key components and materials shall be implemented in accordance with the resolution of the technical expert group of the CNCA.
Refer to Schedule 1 and Schedule 2 for system requirements
6.1.3. Type test items
The type test time is generally 30 working days (when key components and materials need random testing and
When the test time exceeds 30 working days, the maximum time required is calculated). Received samples and/or test
Calculation starts from the date of the inspection fee. Rectification and/or retest by the enterprise due to unqualified data or inspection items
The time is not included in the type test time. In principle, rectification should be completed within 6 months, beyond that period
Limitation is deemed to be the termination of certification.
For accredited bodies recognized by ILAC, laboratories accredited in accordance with ISO /IEC 17025,
In the case of meeting the relevant requirements of the State Accreditation and Certification Commission, you can apply for the use of
Source "method (such as. using production equipment testing (referred to as TMP method), production enterprises witness
Inspection (referred to as WMT method) for type test.
The specific requirements are in accordance with the "Compulsory Product Certification Production Enterprise Testing Resource Utilization Practice" issued by CQC.
Implementation of the Regulations.
6.1.5. Type test report
7. Initial factory inspection
Contents of initial factory inspection
The inspection content includes a full-factor inspection of the factory's quality assurance ability and a certification product consistency check.
The inspection of factory quality assurance ability is based on the "Implementation Rules for Compulsory Product Certification" issued by the CNCA
Requirements for Factory Quality Assurance Ability (No .. CNCA-00C-005) and Audio and Video issued by CQC
Product compulsory certification factory quality control testing requirements "(see Appendix III) implementation.
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