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Combined packaging bag and sterilizing-drying method

A packaging bag and outer packaging bag technology, which is applied in packaging sterilization, packaging, transportation packaging, etc., can solve the problems of substandard moisture, ineffective effect, and difficult control

Active Publication Date: 2009-05-13
江西3L医用制品集团股份有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the conventional treatment method is to first release the E0 residue of the sterilized product, and then use a dryer or an oven to dry the package. Although these methods can dry the product moisture, the effect is not obvious. Difficult to control, often the moisture does not meet the standard

Method used

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  • Combined packaging bag and sterilizing-drying method
  • Combined packaging bag and sterilizing-drying method

Examples

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Embodiment 1

[0017] Such as figure 1 Shown: a combination packaging bag used for sterilization and drying of medical supplies, which is composed of an inner packaging bag 1 inserted into an outer packaging bag 2 .

Embodiment 2

[0019] Such as figure 2 Shown: a method for sterilizing and drying medical supplies using the combined packaging bag described in Embodiment 1, comprising the following steps:

[0020] [1] Put the medical supplies 3 to be sterilized into the aluminum foil inner packaging bag 1 with good barrier force, and set aside;

[0021] [2] Put the inner packaging bag 1 containing the medical supplies 3 to be sterilized into the dialysis packaging bag 2 with good external penetration, and seal the outer packaging bag 2;

[0022] [3] Outer packaging bag 2 is put into sterilization furnace and sterilized with ethylene oxide;

[0023] [4] After the sterilization is completed, raise the temperature in the sterilizing furnace to 70°C, evacuate to a pressure value of minus 60KPA, fill the sterilizing furnace with nitrogen gas with a concentration of 99.999%, keep it for 40 minutes, release the gas and return to normal pressure;

[0024] [5] Repeat step [4] 8 times to fully replace the remai...

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Abstract

The invention relates to a combination packaging bag for sterilizing and drying medical articles and methods of sterilization and dryness. The invention is characterized in that the combination packaging bag comprises an outer packaging bag and an inner packaging bag sleeved in the outer packaging bag. The methods of sterilization and dryness comprise the following steps: putting the inner packaging bag of medical articles to be sterilized into the outer packaging bag; sealing the outer packaging bag by hot pressing; putting the outer packaging bag into a sterilizing stove to sterilize through ethylene epoxide; and then heating up temperature, pumping out vacuum, and charging with nitrogen in the stove; standing for forty minutes; discharging gas, and recovering normal pressure; repeating five to ten times in a way; displacing out residual ethylene epoxide and moisture in the combination packaging bag; taking out the outer packaging bag which is sterilized, and combing and sealing the overlap section between the inner packaging bag and the outer packaging bag, thereby obtaining sterilized and dry medical articles. The invention can exclude the residue amount between the moisture and ethylene epoxide in the combination packaging bag, thereby achieving required standard, and further preventing the medical articles from invalidating due to high moisture during effective lifetime process.

Description

technical field [0001] The invention relates to a packaging bag, in particular to a combined packaging bag used for sterilization and drying of medical supplies and a method for sterilization and drying thereof. technical background [0002] At present, some implantable absorbent products, such as absorbable sutures, absorbable hemostatic materials, etc., are easy to hydrolyze, so after these products are sterilized, not only have strict requirements on the residual amount of E0, but also have strict requirements on the moisture content in the packaging bag. The content is also very strict. If the moisture content in the package exceeds the standard after sterilization, the product will be hydrolyzed by the moisture in the package before use, resulting in product failure. In order to solve this problem, waterproof materials must be used for packaging, but in this way the E0 in the product cannot be released, resulting in excessive E0 residues. In order to solve these two pr...

Claims

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Application Information

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IPC IPC(8): B65D30/10B65D77/04B65B55/18B65B55/00B65B51/10
Inventor 范长权罗响李建芳周平
Owner 江西3L医用制品集团股份有限公司
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