I, strict implementation of the medical device quality acceptance system and medical device warehousing acceptance procedures, is responsible for medical device warehousing acceptance work.
Second, the acceptance of personnel with the arrival notice or with the shipment of the same batch by batch acceptance, sign the entry voucher, and the custodian for the handover procedures. Receiving and inspection personnel on the medical equipment leakage, misdiagnosis of specific quality responsibility.
Three, the acceptance does not meet the acceptance of the content, does not meet the relevant legal standards and quality terms or other suspected quality anomalies of medical devices, fill in the refusal to accept the report form, and notify the Department of quality control to deal with.
Four, the acceptance of medical devices should be packaged, labeling, instructions, and relevant requirements of the supporting documents checked one by one, the whole package should be product certification.
Fifth, acceptance of the first camp varieties, should check the first batch of medical devices to arrive with the batch number of medical devices factory inspection certificate.
Sixth, acceptance of imported medical devices, should check the label of the package whether the Chinese name of the medical device, the main ingredients and import registration number, check the Chinese instructions and legal documents.
VII, fill out the relevant statements and acceptance records in a timely manner, and sign the responsible, according to the provisions of the preservation for inspection.
VIII, consciously study the quality of medical equipment professional knowledge, and strive to improve the level of acceptance work. Purchaser duties to do a good job of user visits, with the relevant personnel to deal with customer inquiries, for quality improvement to provide information on market quality dynamics.