Shanghai Sunland Industrial Co., Ltd is the top manufacturer of Personal Protect Equipment in China, with 20 years’experience. We are the Chinese government appointed manufacturer for government power,personal protection equipment , medical instruments,construction industry, etc. All the products get the CE, ANSI and related Industry Certificates. All our safety helmets use the top-quality raw material without any recycling material.
The patient began to tear the doctor's protective clothing
We provide exclusive customization of the products logo, using advanced printing technology and technology, not suitable for fading, solid and firm, scratch-proof and anti-smashing, and suitable for various scenes such as construction, mining, warehouse, inspection, etc. Our goal is to satisfy your needs. Demand, do your best.
Professional team work and production line which can make nice quality in short time..
The professional team provides 24 * 7 after-sales service for you, which can help you solve any problems
The ,CE, mark affixed to PPE will provide evidence of compliance which product applicable to EU legislation. It indicates risk categories of which PPE is intended to protect users, such as ,protective clothing, complies with Category III is appropriate to prevent death or irreversible health damages. The types of ,CE, standard for ,protective, coveralls
The ANSI/AAMI PB70 ,standard, includes four ,standard, tests to evaluate the barrier effectiveness of surgical gowns, ,isolation, gowns, and surgical drapes. Based on the results of these standardized tests, four levels of barrier performance are defined, with Level 1 being the lowest level of protection, and Level 4 being the highest level of protection.
For ,protective clothing, to pass standard tests, it must meet or exceed minimum requirements of materials’ physical and chemical properties. Once test results are confirmed, it is qualified to carry standard pictogram and need to be correctly identified or labeled on marketing materials.
National, Infection Prevention and Control ,Standards, for Hospitals in Tanzania. are part of the MoHSW’s Quality Improvement Series. All resources in this series are listed below. 1. Tanzania Quality Improvement Framework, September 2004 2. ,National, Infection Prevention and Control Guidelines for Health Care Services in Tanzania, November 2004 3.
11/10/2017, · The good news for exporters is that ,CE certification, covers all of the European Economic Area (EEA), which includes 28 EU countries, as well as Iceland, Lichtenstein, and Norway. “Often the ,CE, marking is described as a trade passport because it enables the free movement of products within the European market," says Han Zuyderwijk, a ,CE, marking expert and president of The Alura Group , based ...
1.1 Scope. 1.1.1* This ,standard, shall specify the minimum design, performance, testing, documentation, and certification requirements for new single-use and new multiple-use emergency medical operations protective ,clothing,, including garments, helmets, gloves, footwear, and face protection devices, used by emergency medical responders prior to arrival at medical care facilities, and used by ...
International ,standards, established by the United Nations Rules for the Treatment of Women Prisoners and Non-Custodial Measures for Women Offenders state that pregnant women should never be placed in solitary confinement as they are especially susceptible to its harmful psychological effects. 20 In addition, placing these women in ,isolation, impedes their access to necessary and timely prenatal ...
CE, marking is only obligatory for products for which EU specifications exist and require the affixing of ,CE, marking. Some products are subject to several EU requirements at the same time. You must make sure that your product complies with all the relevant requirements before affixing the ,CE, marking to it.
Personal ,protective, equipment ,without, the ,CE,-marking may not be sold in the EU. With the ,CE,-mark you will declare that the equipment is in accordance with all legal requirements of the EU market, specifically the European Directive 89/686/EEA. Personal ,Protective, Equipment (PPE) must comply with the new Regulation (EU) 2016/425.
Subpart A - The ,Standard, (§§ 1610.1 - 1610.8) Subpart B - Rules and Regulations (§§ 1610.31 - 1610.40) Subpart C - Interpretations and Policies (§ 1610.61) Figure 1 to Part 1610 - Sketch of Flammability Apparatus; Figure 2 to Part 1610 - Flammability Apparatus Views; Figure 3 to Part 1610 - Specimen Holder Supported in Specimen Rack