Among the various quality indicators for personal lubricant, microbial limits are the "life-or-death red line" for determining product qualification. Due to the unique physiological environment of intimate areas, where the bacterial flora balance is extremely fragile, if the lubricating jelly contains excessive bacteria, molds, or pathogenic bacteria, it can easily lead to user infections, inflammation, and even more serious health problems. Therefore, ensuring the biological safety of every drop of product is a challenge that all compliant production enterprises must overcome.
Microbial control is a systemic engineering effort that cannot be solved by simple post-production sterilization. It runs through the entire product lifecycle: starting with the preparation of production water, which must undergo multi-stage reverse osmosis treatment to meet purified water standards; the air in the production workshop needs to be circulated and purified through high-efficiency filters to control the airborne microbial count; even packaging materials must undergo strict sterilization before use. Negligence in any single step can lead to microbial indicators exceeding limits. The fundamental reason why some low-end products on the market are prone to spoilage and odor is that their production environment does not meet standards, leading to product contamination even before leaving the factory.
A rigorous testing system is the last line of defense for ensuring safety. In regular medical device production processes, each batch of products, once filled, cannot be immediately shipped but must undergo culture tests in a microbiology laboratory. Only when all indicators, such as total bacterial count, coliform bacteria, and Staphylococcus aureus, comply with the "Good Manufacturing Practices for Medical Devices" can the product be released. This "zero-tolerance" attitude towards microorganisms demonstrates the company's ultimate responsibility for consumer health.
PINGCHUANG Medical strictly implements GMP pharmaceutical production standards, with production taking place in a 3,000-square-meter 100,000-grade dust-free purification workshop. We exclusively use medical-grade raw materials and precisely control microbial and heavy metal residues through 21 stringent quality inspection procedures, ensuring the safety and batch stability of every drop of lubricating jelly, allowing your brand to withstand the dual scrutiny of the market and time.
