First, strictly implement the medical device quality acceptance system and medical device warehousing acceptance procedures, and be responsible for medical device warehousing acceptance.
Second, the inspection personnel shall carry out the inspection batch by batch with the arrival notice or the counterparts accompanying the goods, sign the warehousing certificate, and handle the handover procedures with the custodian. Acceptance personnel shall be responsible for the quality of missed inspection and wrong inspection of medical devices.
Three, the acceptance does not meet the acceptance content, does not meet the relevant statutory standards and quality terms or other suspected abnormal quality of medical devices, fill in the rejection report, and notify the quality control department for processing.
Four, the acceptance of medical devices, packaging, labels, instructions and certification documents related to the requirements of one by one to check, the whole package should have a product certificate.
Five, the acceptance of the first camp varieties, should check the first batch of medical devices with the batch number of medical devices factory inspection certificate.
Six, the acceptance of imported medical devices, should check whether the packaging label has Chinese medical device name, main components and import registration number, and check the Chinese manual and related documents of conformity.
Seven, fill in the relevant statements and acceptance records in time, and sign for it, and keep it for future reference according to regulations.
Eight, consciously learn the professional knowledge of medical device quality, and strive to improve the acceptance level. It is the responsibility of the buyer to do a good job of visiting users, cooperate with relevant personnel to deal with customer inquiries, provide dynamic information on market quality and improve quality.