paper sterilization pouches are crucial in industries where maintaining product sterility is paramount, such as in the packaging of medical devices, surgical instruments, pharmaceuticals, and laboratory equipment. The aseptic nature of these pouches helps prevent contamination and ensures the integrity and safety of the enclosed items.
Spec(mm*m) | Qty/carton | packing Size (MM) | G.w(kg) | N.w(kg) |
50X200 | 12 | 420X220X320 | 14.5 | 14 |
75X200 | 8 | 420X220X320 | 14 | 13.5 |
100X200 | 6 | 420X220X320 | 14.5 | 14 |
150X200 | 4 | 420X220X270 | 14.5 | 14 |
200X200 | 2 | 420X220X220 | 10 | 9.5 |
250X200 | 2 | 420X220X270 | 12 | 11.5 |
300X200 | 2 | 420X220X320 | 14.5 | 14 |
350X200 | 1 | 220X220X370 | 8.5 | 8 |
400X200 | 1 | 220X220X420 | 10 | 9.5 |
500X200 | 1 | 220X220X520 | 12 | 11.5 |
A sterilization pouch is typically composed of multiple layers of specialized materials designed to withstand the sterilization process while providing a barrier against microorganisms. The specific composition may vary, but common elements include:
The outer layer is often made of medical-grade paper or Tyvek, a nonwoven synthetic material. This layer allows the penetration of sterilizing agents and provides durability to the pouch.
The inner layer is typically made of a transparent plastic film, such as polyethylene or polypropylene. This layer acts as a barrier to microbial ingress, protecting the contents from contamination after sterilization.
The pouch is sealed using a special adhesive that ensures an airtight and microbial barrier. This seal is crucial for maintaining the sterility of the contents.
Some sterilization pouches include an indicator strip or label that changes color after exposure to the sterilization process, providing a visual confirmation that the pouch has been properly sterilized.
Sterilization pouches often have designated areas for labeling important information, such as the contents, date of sterilization, and expiration date.
These components work together to create a sterile barrier that protects medical instruments and equipment until they are ready for use in clinical or laboratory settings. The materials used are chosen for their compatibility with various sterilization methods, including steam autoclaving, ethylene oxide gas, or other appropriate techniques.
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