[product name] medical absorbent gauze swab

[specification and model] model: type, I; specification: length (1cm-300cm) x width (1cm-300cm) layer (1p-50p). For specific specifications, please refer to the product small package.

[name of registrant] Henan Jianqi medical device Co., Ltd

[address] dingluan Industrial Zone, Changyuan County

[Tel: 0373-8690789]

[after sales service unit] Henan Jianqi medical equipment sales Co., Ltd

[name of manufacturer] Henan Jianqi Medical Equipment Co., Ltd

[address] dingluan Industrial Zone, Changyuan County

[production address] dingluan Industrial Zone, Changyuan County

[contact information] 0373-8690789

[production license] ysyjx production license No. 20080036

[Registration Certificate No.] yxzz 20172640057

[technical requirement No.] yxzz 20172640057

Medical absorbent gauze block

[structure and composition] the product is made of medical absorbent gauze.

[product performance] 1. The product should be folded and flat, without edge exposure (except for the side drawing gauze block), no odor, mildew, impurities, stains and holes; the components can be detected by X-ray with degreasing gauze block, and there is no fracture, no mildew, no hole defect

Drop jumper phenomenon (only applicable to type I gauze block). The tolerance is 2.10% from the actual value. 3. The cotton fiber of degreased cotton yarn should be flat ribbon, 10 μ m to 40 um in width, thickened at the end and with irregular inner cavity

The results show that the dimension should be purple; the fibers should not be dissolved; the solution should not show pink; the warp fibers should be all or almost all cotton fibers, and the weft fibers should be all or almost all typical cotton fibers. When checking warp and weft fibers,

There may be a small amount of isolated foreign fibers occasionally; only a small amount of brown purple fluorescence and a small amount of yellow particles should be observed. Except for a few isolated fibers, it should not show strong blue fluorescence; the number of yarns per 100 mm should meet the requirements of Table 1

The mass per square meter (in gram) shall meet the requirements of Table 1; the minimum breaking force (in Newton) per 50 mm shall meet the requirements of Table 1; the sinking time shall not exceed 10s; the total amount of soluble substances in ether shall not be greater than 0.50%;

After 300S, the height of the surfactant foam should not exceed 2mm; the total amount of soluble matter in water should not be greater than 0.50%; the solution should not be blue, purple, light red or light brown; the color of the obtained liquid should not be deeper than the appendix.

The reference solution Y5 and GY6 specified in a or the control solution prepared according to the following methods: add 7.0ml hydrochloric acid solution (with mass concentration of 10G / L) to 3.0ml primary color solution, and then add hydrochloric acid solution (mass concentration is 10 g / L) to 3.0ml primary color solution

0.5ml of the above solution is diluted to 10.0ml; the mass loss of absorbent cotton gauze shall not be greater than 8.0%; the total sulfate ash content shall meet the requirements of Table 2. 4. The content of x-ray detectable components shall be no less than

55% barium sulfate material or other materials with the same X-ray impermeability, the material should not shed fiber, should not affect the softness of dressing or provide raw material inspection report; gently draw X-ray from gauze bag to detect

The weight of the test assembly shall meet the following requirements: single wire line shall not be less than 0.5 g / M; multi wire line shall not be less than 0.28 g / M; when tested according to Appendix B of yy0594-2006, the image of the sample shall be obviously shallower than the background. 5. Gauze block

There are two types of gauze: sterile and non sterile; gauze block supplied in sterile form shall be sterile. 6. After the gauze block is sterilized with ethylene oxide, the ethylene oxide residue should not exceed 10 μ UG / g.

[scope of application] it is used for clinical wound protection and moisture absorption.

[contraindications] no contraindications.

[precautions] 1. This product is a secondary product. The package is damaged. It is forbidden to use it and destroy it after use.

2. The batch number is shown on the seal or label of the package, and the sterilization date is shown in the outer packing box.

3. The product was sterilized by ethylene oxide.

[usage] 1. Select the applicable specification and model, and open the package after confirming that the outer package is in good condition.

According to the wound surface or fluid exudation of clinical patients, clean the skin, mucous membrane, wound surface and moisture absorption.

3. After the end of use, the product should be treated as medical waste to avoid pollution.

[storage method] 1. This product should be loaded and transported in covered carriage and cabin, and kept clean. It is not allowed to be heavily pressed, directly exposed to the sun, rain or snow.

2. Handle with care to avoid violent collision;

3. The product should be stored away from the fire source, the relative humidity is not more than 80%, no corrosive gas and well ventilated and clean environment.