[product name] medical absorbent gauze pad

[model and specification] model: type I and type II; specification: length (1cm-600cm) × width (1cm-600cm) - layer (1p-50p). See the product small package for specific specifications.

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

[residence] 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

[residence] 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 20172640056

[technical requirements No.] yxzz 20172640056

Medical absorbent gauze pad.jpg

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

[product performance] 1. The product should be folded flat, without burr exposure, odor, mildew, impurities, stains, holes; medical absorbent gauze pad can be detected by X-ray, and there is no breakage, falling off, jumper phenomenon (only applicable to type II gauze pad). 2. The tolerance between actual value and nominal value is ± 10%. 3. The tolerance between actual value and nominal value is ± 10%. 3. The cotton fiber of degreasing cotton yarn cloth should be flat ribbon, 10 μ m to 40 μ m in width, thickened at the end and irregular shape of cavity; the fiber should be purple; the fiber should not be dissolved; there should be no solution showing pink; the warp fiber should be all or almost all cotton fiber, and the weft fiber should be all or almost all typical cotton fiber. In the inspection of warp and weft fibers, a small amount of isolated foreign fibers may occasionally exist; only a small amount of brown purple fluorescence and a small amount of yellow particles should be observed. In addition to a small number of isolated fibers, it should not show strong blue fluorescence; the number of yarns per 100 mm should meet the requirements of Table 1; the weight per square meter (in grams) should meet the requirements of Table 1; the minimum breaking force per 50 mm (in Newtons) should meet the requirements of Table 1; the sinking time should not exceed 10 s; the total amount of soluble substances in ether should not be greater than 0.50%; after 300s, the surface active substances in the test solution should be provided The height of the 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 that of the control solution Y5, GY6 or A prepared by appendix A. 0.5ml of the above solution is diluted to 10.0ml by solution (hydrochloric acid with mass concentration of 10G / L); the mass loss of absorbent cotton gauze shall not be greater than 8.0%; the total amount of sulfate ash shall meet the requirements of Table 2. 4. The x-ray detectable component shall be made of barium sulfate material with the content of no less than 55% or other materials with the same X-ray impermeability. The material shall not shed fiber, and shall not affect the softness of dressing or provide raw material inspection report. The x-ray detectable component shall be gently extracted from the gauze bag and its quality shall meet the following requirements: monofilament: no less than 0.5 The image of the sample should be obviously shallower than the background when tested according to Appendix B of yy0594-2006. 5. The distance between stitches should be no less than 24 stitches per 10 cm. 6. When the suture fluorescent substance is tested according to test a in Appendix D of YY 0594-2006 standard, the suture shall not show strong blue fluorescence; the total amount of soluble matter in water shall not exceed 0.50%. 7. Gauze pad can be divided into sterile and non sterile types; gauze pad supplied in sterile form shall be sterile. 8. The residual ethylene oxide content of gauze pad should not exceed 10 μ g / G after sterilization with ethylene oxide.

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

[contraindications] no contraindications.

[precautions] 1. This product is disposable and its package is damaged. It is forbidden to use it and destroy it after use.

2. See the seal or label of the package for the batch number and the outer packing box for the sterilization date.

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.

2. According to the wound surface or fluid exudation of clinical patients, the clinical operation of cleaning, moisture absorption and other aspects is carried out.

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

[storage method] 1. The product should be loaded and transported in covered carriage and cabin, and kept clean. It should not be under heavy pressure, direct sunlight, 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.