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How our factory uses "surgical grade" standards to protect the innocence of every drop of liquid

Update Date: 2025-03-24 Hit: 19

 In the filling workshop at four o'clock in the morning, the ultraviolet lamp has just completed the last round of disinfection. I squatted under the U-tube holding a sampling bottle, watching the light blue cleaning liquid flow through the mirror stainless steel like a stream - this is a compulsory course before production every day. In an aseptic packaging environment, the fluid pipeline is the blood vessel that transports the lifeline, and no impurities are allowed.

The experience of visiting a dairy factory last month still makes my back cold. The inner wall of their packaging machine pipeline is actually covered with a layer of yogurt scale, like a stalactite cave. When I came back and talked about this with Mr. Zhou from the technical department, he directly slapped our fluid pipeline cleaning standards on the table: "Do you know why the customer specifically asked us to modify the equipment? Just because of this set of cleaning procedures that are more stringent than those in pharmaceutical factories!"

Our factory's aseptic packaging environment management has a "triple barrier". First, the CIP system is intelligently upgraded. Now the cleaning program will automatically match the acid and alkali concentration according to the type of residue. When debugging the new equipment last week, I saw with my own eyes that the system identified the juice sediment and instantly switched to high-temperature pulse mode. Operator Xiao Zhao joked: "This is much smarter than my dishwasher. It even knows to use citric acid to deal with orange juice stains."

Microbial control is even more careless. The new graduate student in the technical department once proposed to shorten the sterilization time, but was speechless by the workshop director Lao Li with experimental data - he compared the two groups of pipelines, and the number of colonies in the standardized cleaning was only a fraction of that in the shoddy group. Now all packaging machine interfaces are designed with quick release, let alone microorganisms, even the floating dust in the air has difficulty finding a hiding place.

What I admire most is the packaging machine compatibility design. Last year, we renovated the production line for a pharmaceutical factory. Their special chemicals would corrode ordinary seals. Our technical team developed food-grade fluororubber accessories that can withstand strong acid cleaning and ensure zero chemical residue. During the acceptance, the quality inspection director of the pharmaceutical factory checked the pipeline with a magnifying glass, and finally said: "Your cleaning standards are enough to be used as a textbook for surgical instruments."

During the night shift, I often see quality inspectors climbing into the equipment interlayer with flashlights. Once I was curious and followed them to see, I found that they were using endoscopes to check the blind spots of the diverter valve. "The sterile packaging environment is not a face-saving project," said Afang, the quality inspection team leader, while adjusting the lens, "These winding pipelines are like the human cecum, which is the easiest to hide dirt."

Recently, a group of Southeast Asian customers came to the factory and stared at our CIP system operation process and recorded videos for half a day. The leading engineer pointed at the packaging machine that was self-cleaning and sighed: "Other manufacturers only talk about equipment parameters, but you even control the shelf life of cleaning consumables." This reminded me of the slogan on the wall of the workshop - "Cleaning is not only a process, but also the conscience of quality."

When changing shifts, I always hear new employees complain about the cumbersome dressing procedures: the headgear must cover all hair, the gloves must be above the elbow, and the shoe covers must be worn in two layers. But once the biological monitor detected excessive microorganisms in someone's cuffs, everyone realized the value of these rules. Now even equipment maintenance is implemented with "medical-grade" management, tools are stored in different areas, and screws for disassembly and assembly have exclusive sterilization boxes.

Standing in the brightly lit workshop, watching the packaging machine swallow and spit out products like a silver dragon, I suddenly understood what the old factory manager often said: "In a sterile packaging environment, every drop of liquid is a breathing life." Those seemingly harsh fluid pipeline cleaning standards are just the most basic respect for these lives. After all, when the consumer tears open the package, what he holds in his hands is not just the product, but also the trust that we uphold day and night.

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