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These are related to the EN455 news, in which you can learn about the latest trends in EN455 and related information industry, to help you better understand and expand EN455 market.
  • What’s the production process of GUSIIE disposable gloves?


    Whichever material rubber gloves are made of, they are manufactured in the same basic way. The process starts with hand-shaped ceramic or aluminum molds on a conveyor, which are dipped in wash tanks with hot water and chlorine or bleach and then dried. This dipping gets rid of any potential residue Read More
  • USA ASTM Standard Compare to Other Country In Medical Gloves


    The following table compares USA ASTM standards to other countries' standards on medical and surgical gloves. Read More
  • Gloves have to meet the requirements which can certification?


    Medical gloves exported to the EU need to meet the requirements of MDR EU No.2017/745 medical devices regulationCommon medical gloves: examination gloves, surgical gloves, laboratory gloves, chemical gloves, mostly disposable glovesCommon medical gloves materials: latex, PVC, nitrile, and composite Read More
  • What is the difference between medical nitrile gloves and civilian nitrile gloves?


    Distinction one: use is different1. Medical gloves are not limited to use in hospitals, as long as the sensitivity of the hand is high, medical gloves can be used.2. Disposable medical examination gloves can be used for "non-medical purposes", but civilian gloves "usually cannot be used for medical Read More
  • What does CE mean?


    What does CE mean? Since 2016, Gusiie gloves have their own export license to the world with its own export license, mainly to North America, Eastern Europe, Southeast Asia, Africa, the Middle East and Western Europe, with an annual output value of 50 million DOLLARS. Production in line with the US Food and Drug Administration specifications and EU CE standards, Swiss SGS certification EN455 certification, EN374 certification and GB 4806.11-2016; In addition, the company has achieved ISO13485 quality system requirements and certification. Read More
  • Why we need ISO 13485 certificate?


    ISO 13485 is the medical device industry’s most widely used international standard for quality management. Issued by the International Organization for Standardization (ISO), the ISO 13485 standard is an effective solution to meet the comprehensive requirements for a Quality Management System in the Read More
  • What’s the EN455 standard?


    EN 455 Parts 1 to 4: 2000 to 2009 is a standard of Medical gloves for single use. This includes tests to assess the freedom from holes which is based on a penetration resistance test similar to that of EN 374 Part 2, plus tests to assess the dimensions of the gloves and the mechanical strength. Read More
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