Q & A
What is CCC certification?China Quality Certification Center ( abbreviation CQC) is a professional certification body
approved the establishment of national authorities .
CQC and its branches are located in China and abroad to carry out certification work
earlier certification authority , for decades has accumulated rich experience in
certification , various businesses are outstanding results . Currently , CQC at home
and abroad a total of 45 branches and more than 200 contract testing laboratories ,
certification and signed cooperation agreements with 22 foreign certification bodies ,
with more than 7300 professional full-time , part-time auditors, inspectors and
technical experts , and has a strong teaching force . Comprehensive network of
services , to provide customers with timely, thoughtful , high-quality service .
CQC is the representative of China's accession to the International Electrotechnical
Commission IEC Conformity Testing and Certification Organization (IECEE) Multilateral
Recognition (CB) national certification body system (NCB), is to join the International
Certification Network (IQNet) and the International Federation of Organic Agriculture
Movements (IFOAM) national certification bodies, international mutual recognition
between business and foreign many well-known CQC certification bodies , as well as
extensive international exchanges , so that CQC has won a good international image.
Quality service, strong technical force , advanced management level to ensure the
smooth conduct of business CQC , CQC quality objectives for the successful realization
of this brand is well-known CQC certification bodies provide a strong guarantee.
CQC 's quality policy : fairness norms honest and efficient high-quality science and
CQC quality goal : to become one of the leading brands in the world certified in the field ,
continuing to provide customers with value-added authentication services.
What is REACH certification?EU regulation REACH certification is "Chemicals Registration, Evaluation, Authorisation
and Restriction" (REGULATION concerning the Registration, Evaluation, Authorization and
Restriction of Chemicals) for short, is the establishment of the European Union, chemical
and since June 1, 2007 implementation product regulatory system.
The new EU chemicals policy, REACH certification (Chemicals Registration, Evaluation
and Authorization), the purpose of a high level of protection of human health and the
environment while promoting innovation and green chemicals.
December 18, 2006 EU regulation (EC) No.1907/2006 registered on chemicals, evaluation,
authorization and restriction, December 18, 2006 the EU Council Directive 2006/121/EC
modified by Commission Directive 67/548/EEC (classification of dangerous substances,
packaging and labeling) on December 30, 2006 published in the official Journal.
REACH will be implemented on June 1, 2007, will replace the nearly 40 existing EU
regulations and directives, to provide a simple system with a better way to manage chemicals.
What is VDE certification?VDE certification stands for Prufstelle Testing and Certification Institute, which means
the German Institute of Electrical Engineers . Directly involved in the German national
standards , VDE consists of approximately 30,000 organizations and individual members .
These members mainly from the federal government / organizations representing each
state / industry research institutions .
VDE Testing & Certification Institute (VDE Testing and Certification Institute) is located in
Offenbach, Germany offerbach is a German Institute of Electrical Engineers Association
(Verband Deutscher Elektrotechniker, referred to as VDE) belongs, was founded in 1920 .
As a neutral and independent body . VDE laboratory based applications , according to
German VDE standards or European standard EN or IEC International Electrotechnical
Commission standards for inspection and certification of electrical products , is one of
the prestigious European certification bodies in the world 's most experienced . It is
nearly 2200 customers each year and 2,700 German companies in other countries to
complete a total of 18 000 certification program. So far, nearly 50 countries worldwide
the 200,000 kinds of electrical products have VDE mark. In many countries, VDE
certification mark is even more famous than their own certification mark , especially
importers and exporters to be recognized and valued.
After VDE laboratories in accordance with the strict standards testing and certification
of products, consumers can rest assured .
Survey results showed that: 62% of Germans already know VDE mark , which thus
became one of the most famous security token . Most people think of safety markings
on the importance of electrical supplies in Germany, people familiar with the VDE
mark has a 77% holding this attitude. 73% of German citizens considered by a neutral
body to conduct security checks "important" or " very important " for electrical products.
Certification and inspection is one of Europe's most testing organizations test
experience , is authorized by the European Union and the International CB CE Notified
Body members . In Europe and internationally , electrical products get the CENELEC
European certification system , approved CECC electronic components Harmonized
system of quality assessment in Europe , the worldwide IEC electrical products,
electronic components , such as the certification system . The product is widely used
to assess household and commercial uses , including electrical , IT equipment ,
industrial and medical technology equipment , assembly materials and electronic
components , wire and cable.
What is "Medical Device CE certification" certification?Medical equipment products to be passed CE certification, need to do work in three areas .
First, the collection and certification of products related to EU technical regulations and
European (EN) standards, through digestion, absorption, into the enterprise product
Second, enterprises in strict accordance with the above product standards organization of
production, that is, the above-mentioned technical regulations and EN standards, implement
enterprise product design and development and manufacturing of the entire process .
Third, companies must build and maintain the standard ISO9000 + ISO13485 quality system
and obtained ISO9000 + ISO13485 certification.
Medical Device CE certification should follow the EU technical regulations and EN standards.
For the EU published Directive 18 categories of industrial products from these directives
structure, they can be divided into vertical and horizontal directive instruction . Vertical
instructions are specific products for the object, such as the Medical Device Directive ;
horizontal directive applies to all kinds of products , such as electromagnetic compatibility
directive , which applies to all electrical and electronic parts and components.
For medical devices , the applicable directives has fourteenth , the first and fifth ,
namely : 93/42/EEC Medical Device Directive , 73/23/EEC Low Voltage (LVD) Directive
89/336/EEC Electromagnetic Compatibility Xing (EMC) directive .
EU standards support these commands are:
(1) EN60601-1 Medical Electrical Equipment Part I: General requirements for safety ;
(2) EN60601-1-1 Medical Electrical Equipment Part I: General Requirements for Safety
and First Amended ;
(3) EN60601-2-11 Medical electrical equipment Part II : γ beam therapy equipment safety
(4) EN60601-1-2 Medical Electrical Equipment Part I: General Requirements for Safety
1.2 Parallel standard Electromagnetic compatibility - Requirements and tests.
The first ( 1 ) , ( 2 ) , ( 3 ) criteria is Gamma Knife Low Voltage (LVD) test based on:
No. ( 4 ) criteria is Gamma Knife electromagnetic compatibility (EMC) test basis.
What is PSE certification?In 1995, Japan enacted a new law banning products , the new regulations no longer
follows the principle of error -party liability , and the use of European and North
American practice ( innocent party liability principle ) , the party responsible for product
safety requirements for the product manufacturers, importers Manufacturers ,
distributors and so on.
April 1, 2001 , before the Japanese Electrical Appliance and Material Control Law
(DENTORI) will control the products are divided into A, B two categories, wherein,
A class includes 165 kinds of products , mainly in the power cord, fuses, switches ,
transformers , ballast , etc. ;B class includes 333 kinds of products, mainly lighting,
household appliances , office equipment. Class A products must obtain government
mandatory certification , namely T flag , and the flag is only by MITI ( MITI ) issued .
Class B product conformity shall be made self-proclaimed or apply for third-party
certification , such as TUV Rheinland can mark the S flag .
After 1 April 2001 , Electrical Appliance and Material Safety Law (DENAN) replaces
DENTORI France , while Japan has abolished the T flag , the government no longer
issue certificates directly , but to authorize a third party certification body for product
conformity assessment tests.
New regulations the product is divided into " specific electrical and Materials " and "non-
specific electrical and Materials ." The " specific electrical and Materials " includes a total
of 112 kinds of products ; "non-specific electrical and Materials " includes 340 kinds of
products. To enter the Japanese market, " specific electrical and Materials " products
must obtain third-party certification , labeling PSE ( diamond ) symbol ; "non-specific
electrical and Materials " products shall be made self-proclaimed or apply for third-party
certification , labeling PSE ( Round ) sign.
New law reduced the number of categories of products , more products are classified as
non- classified products " and no longer subject to DENAN constraints, and some
previously classified as "A Class " products are now classified as " specific electrical
and Materials ."
What is E-MARK certification?E / eMark detection is the European Common Market, on the steam locomotive spare parts
and security products, noise and emissions, are required to act in accordance with the EU】
【EEC Directives and the Economic Commission for Europe Regulation ECE Regulation】
【requirements through product meets testing requirements, namely to grant a certificate
to ensure traffic safety and environmental protection requirements.
E-Mark detection by testing different country, the number granted is different, for example,
apply to Luxembourg, the E-Mark logo E13/e13.
Applicable product range
Vehicle - that is two or three or more moving motor vehicles, such as passenger cars,
trucks, motorcycles, buses and road vehicles outside the steam locomotive components
- lights and bulbs, a variety of mirrors, tires, wheels, brakes, horn, anti-theft devices, seat
belts, automotive glass and exhaust pipe.
Steam locomotive spare parts - helmets, child safety seats, car electrical products
Since October 2002, to require all vehicles, vehicle parts, and electronic products for
the car must be enforced EMC testing.
All electronic components sold in Europe must comply with the EMC Directive unified
95/54/EC, the EMC Directive 89/336/EEC the self-declaration is no longer valid. Vehicles
authorized by the EU institutions issued a notice products E / e Mark certification. In other
words, vehicle electronics and electronic components for the original CE (EMC) testing from
October 2002 onwards no longer valid. European countries must re-apply for Department of
Transportation issued E / e Mark certificate for their sales in the European market.
What is FCC certification?FCC (Federal Communications Commission, the U.S. Federal Communications
Commission ) established in 1934 by COMMUNICATIONACT is an independent U.S.
government agency , directly responsible to Congress . FCC control of radio, television ,
telecommunications, satellite and cable to coordinate domestic and international
communications. Involving the United States more than 50 states, Colombia and the
United States respective districts, to ensure life and property of the radio and wire
communications product safety , FCC 's engineering department (Office of Engineering
and Technology) is responsible for the Commission's technical support, and is
responsible for equipment accreditation matters. Many wireless applications ,
communications products and digital products to enter the U.S. market, require FCC
approval. FCC Commission to investigate and study the various stages of product
safety to find the best way to solve the problem , but FCC also include radios ,
According to the relevant parts of the United States Federal Communications Regulations
(CFR 47 part ) stipulates that where electronic products into the United States needs to
be EMC certification ( some of the relevant provisions of the special provisions of the
products ) , one of the more common authentication method , there are three :
Certification, DoC, Verification. These three product certification methods and procedures
are quite different , different products can choose the authentication method in the FCC
with the relevant requirements. Decreasing its certification rigor .
Federal Communications Commission (FCC) ---- managed import and use of radio
frequency devices, including computers, fax machines, electronic devices, radio reception
and transmission equipment, radio controlled toys, telephones, personal computers and
other products that may harm personal safety. If you want to export these products to
the United States, must be authorized by the government of the laboratory according to
FCCtechnical standards for testing and approval. Importers and customs agents to
declare each radio frequency device complies with FCC standards, the FCC license.
For the FCC certification, different products have different each of the three
authentication modes, namely: Verification, Declaration of Conformity (DoC), Certification.
erification is the manufacturers are free to take certain steps to ensure that products
meet appropriate technical standards process.
Declaration of Conformity by the responsible party to take certain steps to ensure that
products meet appropriate technical standards process.
FCC Certification is based on test data and signed application and device approval process.
What is GS certification?GS is the meaning of German "Geprufte Sicherheit" (security certified), there are
also "Germany Safety" (German security) mean. GS certification to the German Product
Safety Act (SGS) as the basis, in accordance with the European harmonized standards
or the German industrial standard DIN EN testing of a voluntary certification is recognized
in Europe German safety certification mark.
GS certification mark indicates that the product has passed the safe use of the credibility
of an independent agency of the test. GS certification mark, although not legally required,
but it does in the product malfunctioning caused by accident, so that manufacturers are
subject to strict German (European) product safety laws. So GS certification mark is a
powerful marketing tool that can enhance customer confidence and desire to buy.
Although the GS is a German standard, but most countries in Europe agree. And at the
same time meet the GS certification, the product will meet the requirements of the EC
CE mark. Not the same and CE, GS certification mark does not legally required, but
because of security awareness has penetrated ordinary consumers, an electrical GS
certification mark may be more general in the market more competitive products.
You can apply for GS certified products:
Household appliances, such as refrigerators, washing machines, kitchen
appliances and so on.
Home electronics devices, such as audio-visual equipment.
Electrical and electronic office equipment such as copiers, fax machines, shredders,
computers, printers and so on.
Industrial machinery, laboratory measuring equipment. Other security-related products
such as bicycles, helmets, ladders, furniture and so on.
GS certification mark
GS Mark certification can be issued: TUVRH, TUV-SUD, VDE, NEMKO, UL-DEMKO
What is ROHS certification?EU ROHS certification (Restriction of Hazardous Substances Directive) has been scheduled
for July 1, 2006 implementation, since that date, all electrical and electronic equipment sold
in Europe of restricted hazardous substances must comply with the stringent requirements
of Directive .
The Directive stipulates that the European sales of electrical and electronic products, lead
Pb, cadmium Cd, mercury Hg, hexavalent chromium Cr6 +, PBBs PBBs, PBDEs PBDEs
six hazardous substances be restricted after more harmful substances will also be
RoHS certification covers the range of AC1000V, DC1500V following directories listed by the
electronic and electrical products:
Large household appliances: refrigerators, washing machines, microwave ovens,
Lighting: In addition to outside the household fluorescent lighting, lighting controls
air conditioners and other.
Large household appliances: refrigerators, washing machines, micro and small household
appliances: vacuum cleaner, iron, hair dryer, oven, watches and other wave oven,
air conditioning, etc.
IT and telecommunications equipment: computers, fax machines, telephones, cell phones,
Civilian devices: radios, televisions, video recorders, musical instruments, etc.
Lighting: In addition to outside the household fluorescent lighting, lighting controls
Power Tools: drills, lathes, welding, spray, etc. (to be installed except for large-scale
Toys / entertainment, sports equipment: electric cars, video game.
Medical Devices: radiation therapy, ECG testing, analysis equipment, etc.
Monitor / control devices: smoke detectors, incubators, plant monitoring and control
Which, RoHS Directive currently applicable 8,9 two.
RoHS certification (2002/95/EC) on the maximum allowable concentration of harmful
substances (threshold): Cd threshold of 100ppm; Pb, Hg, Cr6 +, PBB, PBDE threshold
1000ppm; their testing method also requires countries to coordinate.