non woven series-尊龙凯时官方旗舰店

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

[product performance] 1. this product should be folded and flat, without any rough edges, no odor, no mildew spot, impurities, stains, holes and other defects. 2. medical absorbent gauze bag x-ray detectable components without fracture, fall off, jump line phenomenon (only applicable to ⅱ type gauze bag). 3. the cotton fiber should meet the requirements of the identification test a, b and c when the medical absorbent gauze is used according to the test of yy 0331-2006. according to the 5.3 test of yy 0331-2006, the solution should not be pink. according to the test of yy 0331-2006, only a small number of isolated foreign fibers are allowed to exist. the cotton and viscose gauze should meet the requirements of yy 0331-2006. according to the 5.6 test in yy 0331-2006, the yarn number of 100mm should meet the requirements set out in table 1 and table 2 of yy 0331-2006. according to the test of yy 0331-2006, the quality of each square metre (in grams) should comply with the requirements of yy 0331-2006 standard table 1 and table 2. according to the 5.8 test in yy 0331-2006, the minimum breaking force of 50mm (in newtons) should meet the requirements of yy 0331-2006 standard. according to the 5.9 test of yy 0331-2006, the subsidence time should not exceed 10s; according to the 5.10 test of yy 0331-2006, the total amount of soluble in ether should not be greater than 0.50%; according to the test of yy 0331-2006, the height of the surface active substance foam on the surface of the test liquid after 300s should not exceed 2mm; according to the test of yy 0331-2006, the total amount of soluble in water should not be greater than 0.50%. the solution should not be blue, purple, light red or light brown according to the 5.13 test of yy 0331-2006. according to the test of yy 0331-2006, the color of the liquid obtained should not be darker than the control liquid specified in appendix a. according to the 5.15 test of yy 0331-2006, the quality loss of absorbent cotton gauze should be no more than 8.0%; the quality loss of cotton viscose blended yarn should not be greater than 11.0%; according to the test of yy 0331-2006, the total amount of sulphate ash should meet the requirements of table 3 of yy 0331-2006. 4. x-ray detectable components shall be made of impenetrable materials, which shall not be stripped of fiber and shall not affect the softness of the dressing. 5. gently extract the x-ray detectable component from the gauze package to indicate its quality, which should meet the following requirements: single wire: not less than 0.5 g/m; multifilament: no less than 0.28 g/m.

[scope of application] for clinical nursing and moisture absorption.

contraindication: no absolute contraindication.

1. this product is a disposable product, which is damaged in packaging and is strictly prohibited to be used and destroyed after use.

2. see packaging seal or label on the production batch number, and the sterilization date is in the outer packing box.

3. this product is sterilized by ethylene oxide.

[use method] 1. select the applicable specifications and model, and then open the package after the outer packing is in good condition.

2. according to the clinical patients' wound, or the exudation of the body fluid, the product size can be used to protect the wound and moisture absorption.

3. after the product is finished, it should be treated with medical waste to avoid pollution.

[storage method] 1. this product is used in the carriage and hold of the cabins, and is kept clean, without pressure, sunshine and rain and snow.

2. handle gently in handling and avoid violent collision;

3. the product shall be stored away from the fire source, and the relative humidity shall not exceed 80%, without corrosive gas and well-ventilated and clean environment.

[production date] see packaging seal or label.

expiry date: see packaging seal or label.

[label, package logo]