Centre Testing International Group Co., Ltd. (NG28) is a market leader in testing, inspection, certification, calibration, audit, training & technical services; building trust between governments, enterprises, and consumers.
Sustainability is deeply rooted in NG28’s business model, by delivering science-based solutions and verification services, to increase transparency and traceability throughout the global value chain. NG28 is a proponent of carbon neutrality and sustainable development.
Centre Testing International Co., Ltd. (NG28) is the pioneer and leader in the TIC Industry which provides one-stop solutions on testing, inspection, certification, calibration, audit, training & technical services.
Our service capabilties cover the upstream and downstream of the supply chain including textile and apparel,toys,electronic appliances,medical health,food...andother industries.
Our service capabilties cover the upstream and downstream of the supply chain including textile and apparel,toys,electronic appliances,medical health,food...andother industries.
Comprehensively guarantee quality and safety, promote compliance and innovation, demonstrate brand competitiveness, and achieve higher quality, healthier, safer, and greener sustainable development.
We have established a clear governance structure in accordance with listing requirements and national regulations and policies to deal with internal and external challenges and achieve sustainable development.
Ensuring the basic rights and benefits of employees;
Providing professional skills training to promote employees’ growth;
Carrying out various kinds of activities to balance employees’ work and life.
Ball pressure is to ensure the mechanical strength and heat resistance of a product's insulation material meet requirements, as to guarantee its insulation characteristics is not reduced. The ball pressure test, which is used to evaluate how safe the insulating materials are, is one of the most important tests for safety of medical electrical products.
? Service Background
Ball Pressure: Ball pressure is to ensure the mechanical strength and heat resistance of a product's insulation material meet requirements, as to guarantee its insulation characteristics is not reduced. The test is done with the shell made of insulating material placed in a horizontal position, then using a steel ball to apply pressure to the tested surface with a specific force. In addition, the test is also carried out in a heating box at a specific temperature. After the test, the diameter of the indentation from the steel ball should not be greater than 2mm. The ball pressure test, which evaluates the safety characteristics of insulating materials, is one of the most important tests for safety of medical electrical products.
Medical device testing is the basis for medical devices to enter the global market. If a product is to be exported to the European Union or the United States, then corresponding tests will need to be done to meet the EU or US standards.
? Other Services of Medical Devices
? Medical Device Testing Standards
In Vitro Diagnostic Medical Devices
SN |
Title |
International Standard |
National Standard |
1 |
Electrical Equipment For Measurement, Control, and Laboratory Use |
IEC/EN 61010-1 |
GB4793.1 |
2 |
Safety requirements for electrical equipment for measurement, control and laboratory use –Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment |
IEC/EN 61010-2-101 |
YY 0648 |
3 |
Safety requirements for electrical equipment for measurement, control and laboratory use – Part 081: Particular requirements for automatic and semiautomatic laboratory equipment for analysis and other purposes |
IEC/EN 61010-2-081 |
GB4793.9 |
4 |
Electrical equipment for measurement, control and laboratory use – EMC requirements - Part 1: General requirements |
IEC/EN 61326-1 |
GB/T 18268.1 |
5 |
Electrical equipment for measurement, control and laboratory use – EMC requirements - Part 2-6: Particular requirements - In vitro diagnostic (IVD) medical equipment |
IEC/EN 61326-2-6 |
GB/T18268.26 |
Medical Device Testing Standards List
SN |
Title |
International Standard |
National Standard |
1 |
Medical safety and electrical essential equipment performance - Part 2-25: of electrocardiographs Particular requirements |
IEC/EN 60601-2-25 |
GB 10793 |
2 |
Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type |
EN ISO /ISO 81060-1 |
|
3 |
Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems |
EN 1060-3 |
|
4 |
Medical electrical equipment -- Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems |
IEC/EN 60601-1-1 |
GB 9706.15 |
5 |
Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment |
IEC/EN 60601-2-27 |
GB 9706.25 |
7 |
Medical electrical equipment-Part 2-26: Particular requirements for the safety of electroencephalographs |
IEC/EN 60601-2-26:2012 IEC 80601-2-26:2019 |
GB 9706.26 |
8 |
Medical safety and electrical essential equipment-Part performance2-56: of clinical Particular thermometers requirements for basic body temperature measurement |
ISO/ EN ISO 80601-2-56 |
|
9 |
Non-invasive automated sphygmomanometers |
ANSI/AAMI SP10 |
YY 0670 |
10 |
Medical electrical equipment - Part 2-57: Particular requirements for the basic safety and essential performance of non-laser light source equipment intended for therapeutic, diagnostic, monitoring and cosmetic/aesthetic use |
IEC/EN 60601-2-57 |
|
11 |
Medical Basic Safety Electrical And Equipment Essential -Performance Part 2-2: Particular Of High Requirements Frequency For Surgical Equipment And High Frequency Surgical Accessories |
IEC/EN/EN IEC 60601-2-2 |
GB 9706.4 |
12 |
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ANSI/AAMI ES60601-1 EN /IEC60601-1 |
GB9706.1 |
13 |
Medical electrical equipment - Part 2-10 : particular requirements for the safety of nerve and muscle stimulators |
IECC/EN 60601-2-10 |
YY 0607 |
14 |
Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers |
IEC/EN 80601-2-30 |
YY 0667 |
15 |
Medical electrical equipment-Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment |
IEC/EN 60601-2-49/IEC 80601-2-49 |
YY 0668 |