Medical sterile cartridge needle box preservation time

1. Hospitals purchasing disposable sterile medical supplies, must be obtained above the provincial level drug supervision department issued "medical device manufacturer license", "industrial products production license", "medical device product registration certificate" and health administrative department issued health permit approval of the production enterprise or obtain "medical device business enterprise license" business enterprises to purchase qualified products. Imported disposable catheters and other sterile supplies should have the "medical device product registration certificate" issued by the State Council's drug administration department, the supplies should have the sterilization date and expiration date and other Chinese markings. 2. Disposable sterile medical supplies are uniformly purchased by the Equipment Section, and the user departments are not allowed to purchase on their own. Each purchase by the equipment section must be carried out in accordance with the procurement system, strict quality control.

3. Aseptic supplies have a person responsible for the establishment of a register, including: supplier, manufacturer, name of the supplies, quantity, specifications, batch number, sterilization expiration date, the relevant certificate number, the operator, signature and so on. Receiving single-use sterile medical supplies to have received registration records.

4. Sterile supplies stored in a ventilated, dry and cool room shelves, from the ground ≥ 20CM, from the wall ≥ 5CM. Strictly prevent packaging damage, failure, mold, and strictly prohibit the use of substandard supplies issued by the department.

5. Unqualified products or products of doubtful quality are found, should immediately stop using, report to the pharmacovigilance management department, shall not be returned for processing. Before use, we should check the small package is not broken, failure, the product is not clean. Do one needle, one tube, one person to use.

If pyrogenic reactions, infections or other abnormalities occur during use, samples must be retained and sent for testing, detailed records in accordance with the provisions of the report of the hospital infection management.

. Disposable sterile supplies after use is prohibited re-use and return to the market.

1. Each department must strictly carry out the classification of domestic garbage and medical garbage in accordance with hospital regulations.

2. All toxic and hazardous waste items are classified by the department and then collected and disposed of by specialized personnel.

3. Living garbage is placed in black plastic bags sealed delivery, medical waste and toxic, hazardous waste placed in yellow plastic bags sealed delivery.