基本信息
Crafted for sterile pharmaceutical production, this pharmaceutical grade 316L stainless steel sieve mesh meets strict FDA, GMP, and USP Class VI standards, supporting compliance with global drug manufacturing regulations. It is designed to address core challenges in pharmaceutical processing, including microbial contamination risks, low filtration efficiency of sterile powders, and difficulty in validating cleaning processes. The product undergoes gamma irradiation sterilization before delivery, helping reduce the need for on-site sterilization and lowering production downtime. Its smooth, non-porous surface and corrosion-resistant properties support CIP (Clean-in-Place) and SIP (Sterilize-in-Place) operations, helping simplify cleaning validation procedures for pharmaceutical manufacturers. It is suitable for sterile drug powder screening, injectable liquid filtration, and biopharmaceutical cell culture separation, helping maintain product purity and support regulatory compliance.
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