The ultra-fine fiber IPA low endotoxin sterile wiping cloth is made of 80% knitted polyester and 20% polyamide fiber, pre wetted with a mixture of 70% isopropanol and 30% water for injection (WFI), which can control contamination and ultimately maintain compliance with dynamic pharmaceutical production management standards (cGMP), while consuming less resources. The wiping cloth is made of polyester and polyamide fiber split ultrafine fibers, which improves the cleaning effect and pollutant adsorption ability. It has strong adsorption properties and can quantitatively release solvents to the surface. Compared with other pre wetting cloths, it can cover a larger area. The ultra-fine fiber wiping cloth is pre wetted with 70% isopropanol solution and 30% water for injection (WFI). The wiping cloth has been verified to have a sterility level of 10-6, ensuring sterility

• Polyamide fiber splitting ultrafine fibers can improve cleaning efficiency and pollutant adsorption capacity, and can deposit solvents smoothly and uniformly on the surface.
• Compared to non microfiber wiping cloths, it can cover a larger surface area, thereby reducing the number of wiping cloths required for some cleaning tasks.
• Pre wetting cloth with controllable saturation can reduce solvent usage, VOC, and consumption.
• Verified sterility level can reach 10-6 sterility assurance level, suitable for Class A and Class B clean rooms.
• Support customization of various size specifications.

Meet the strict requirements for microbial contamination control in the pharmaceutical and biotechnology industries, designed specifically for GMP compliant Class A to Class B clean areas.

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