1.Powdered or Powdered free .
2.Yellow colour ,hospital medical examination or cleaning glove and others.
3. CE,FDA510K ,EN455,EN374,ISO9001,ISO13485 Certifications etc.
4.AQL:1.5,2.50,4.0 ;Medical grade and Industrial grade ,food grade ,electronic grade etc.
5.Size: S,M,L,XL,XL etc. and weight as your requirement.
6.no latex and non sterile
7.beaded cuff;sigle use only
8.soft and comfortable.
9.OEM or ODM packing.
10.usage widely for hospital medical examination,health care,hotel ,restaurant ,home cleaning etc
Yellow Vinyl Glove Yellow Vinyl Glove,Hotel Glove,Yellow Disposable Vinyl Gloves,Yellow Color Vinyl Gloves Zibo Hongye Shangqin Medical Science and Technology Co.,Ltd. , https://www.vinylgloves.cn
The meaning of CE certification
The meaning of CE certification
"CE" is an abbreviation of "Conformite Europende" and is a mandatory safety mark for the EU. It is established by the European Commission to define technical regulations that limit the basic sales conditions of manufacturers and importers of products in the European market to ensure the safety and health of users. At present, the countries that recognize the CE mark are: Austria, Belgium, Denmark, Britain, Finland, France, Greece, Italy, Ireland, the Netherlands, Portugal, Spain, Norway and other 18 countries and Czech, Hungary, Poland, etc. wishing to join the EU 5 country.
The characteristics of "CE" and the benefits of implementing "CE" "CE", as a mandatory safety mark for the EU, is regarded as a "passport" for Chinese products to enter the EU market. The EU countries have specialized inspection agencies to inspect the products circulating on the EU market through various channels. Once the products are found to be inconsistent with the requirements of the EU Directive, the importers or manufacturers will be severely punished. Tens of millions of euros.
Domestic companies rarely produce directly in accordance with CE's testing standards - European harmonized standards or national standards, and the specific requirements of the standards are not clear. Therefore, in order to reduce the risk, the manufacturer usually asks a third-party certification body to test, verify the conformity of the product, and issue supporting documents. Among them, the number of announcements (that is, NOTIFIED BODY designated by the competent authorities of various countries and recognized by the European Commission) is the most authoritative. The advantages are:
1. Ensure that the products produced meet the requirements of European harmonized standards;
2. Gain maximum trust from customers or importers;
3. Maximize the trust of market surveillance agencies to reduce the risk of being found to be incompatible with safety and health requirements;
4. Effectively prevent the occurrence of various allegations, such as allegations of consumer associations or similar protection groups and allegations of competition for competition, and provide favorable evidence in the face of litigation.