non woven series-尊龙凯时官方旗舰店

[structure and composition] this product is made of non-woven fabric with special finishing.

1. the appearance shall be dry, clean and without mold, and the surface shall not allow adhesions, cracks, holes and other defects; the joints can be machined by stitching, bonding or heating. the needle should be sealed, the needle should be 8 to 14, and the stitch should be uniform, straight, and no jumping needle. the parts should be flat, sealed and free of bubbles after the processing of adhesion or heat treatment. the zipper can not be exposed, and the pull head should be self - locked. 2. the protective clothing consists of a hooded jacket and trousers, which can be divided into a body structure and a split structure; the structure should be reasonable, easy to wear, and close in combination. the cuff and ankle are elastic, and the face of the cap and the waist are elastic. 3. the model specifications are divided into: 160, 165, 170, 175, 180 and 185, as shown in table 1 and table 2 of product standards. 4. the hydrostatic pressure of the key parts is not lower than 1.67kpa (17cmh2o); moisture transmission should not be less than 2500 g / ㎡, d); resistance to synthetic blood penetration should not be lower than the level 2 requirements in table 3 of the product standard; the water level should not be lower than level 3. 5. the fracture strength of the material in key parts should not be less than 45n. 6. the breaking elongation of the material in the key parts should be no less than 15%. 7. the filtration efficiency of non-oily particles should not be less than 70% for the key parts and joints. 8. the damage length of flame retardant property is not greater than 200mm; the renewal time shall not exceed 15s; the smoldering time is not noisy 10s. 9. the charge should not be greater than 0.6uc/ piece. 10. the electrostatic attenuation time shall not exceed 0.5s. 11. the primary stimulus should not exceed 1. 12. microbiological indicators should meet the requirements of microbiological indicators in gb15979-2002, and see table 4 in the product standard. 13. the residual amount of ethylene oxide should not exceed 10ug/g.

[scope of application] for clinical medical staff to be exposed to the blood, body fluids, secretions, etc. of patients with potential infectious diseases.

contraindication: no contraindications.

1. this product belongs to disposable products, which is strictly prohibited to use.

2. if the production batch number and expiry date are shown in the packaging seal or label, the sterilization date is in the outer packing box;

3. ensure the packaging is in good condition before use, and the product is in the valid period;

4. this product is for external use. please destroy it after use.

1. open the product packaging bag, remove the protective clothing and open the zipper;

2. extend the opening of the zipper from the opening to the legs, then wear the jacket, and the hand is extended from the sleeve, and the gloves are pulled.

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

[storage method] 1. the product is used in the carriage and hold of the cabins, and is kept clean, without pressure, sunshine and rain or 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 the packing seal or label.

expiry date: see the packing seal or label.

[label, package logo]