Supply side (hereinafter referred to as Party A):
Purchasing side (hereinafter referred to as Party B):
In order to strengthen the quality management of medical devices, to ensure the quality of the device, to protect the two sides of the *** with the interests of the maintenance of consumer rights and interests, A, B and the two sides in the spirit of equality, the principle of cooperation, signed the following quality assurance agreement:
A, B must be fully licensed legitimate business enterprises, that is, with a drug and device business enterprise license, business license, medical device registration certificate and other necessary certificates and permits. Party A must provide the purchase and sale of equipment personnel of the legal person power of attorney and the commission time limit, a copy of the ID card, so that Party B for the record.
Second, the supplier to ensure that the quality of the instruments operated in accordance with national standards for devices (is013485). Goods inside and outside the packaging and instructions must comply with the relevant state regulations.
Third, Party A to Party B in the packaging of the goods supplied by the quality of medical devices must meet the requirements of the packaging is solid, in line with the requirements of storage and transportation, and Party B's storage and transportation conditions should be in line with the conditions of the medical equipment required, the delivery of goods such as storage and transportation due to the economic losses caused by improper Party B is responsible for.
Fourth, Party B received the goods shipped by Party A, should be timely acceptance, such as the discovery of goods missing, damaged, etc. should be promptly notified to Party A to deal with.
Fifth, Party B in the operation or use of medical equipment provided by Party B in the event of quality problems, should provide detailed and certain quality information, and actively cooperate with Party A to do a good job in the investigation and evidence collection and aftercare work.
Sixth, the above provisions of the unresolved issues, agreed by consensus by both parties.
VII. This agreement shall come into force after confirmation and sealing by both parties.
VIII, this agreement in duplicate, A, B and each party to sign a copy.
IX, the validity of this agreement: ___ years ___ months ___ to ___ years ___ months ___.
Party A (seal): Party B (seal):
Date:
Medical Equipment Quality Assurance Agreement 2(supply side) Party A:
(demand side) Party B:
In order to ensure that the A and B sides of the operating medical devices, product quality, protect the legitimate rights and interests of consumers. In order to ensure the quality of products, safeguard the legitimate rights and interests of consumers, improve product quality and service level, clear product quality responsibility, strengthen friendly cooperation, in accordance with the "Product Quality Law", "Regulations for the Supervision and Administration of Medical Devices" and other relevant state laws and regulations, by consensus, the A and B reached the following agreement:
A. Party responsibility
2, Party A's business personnel should be stamped with Party A's official seal and signed by Party A's legal representative of the original power of attorney and a copy of his identity card, and strictly in accordance with the power of attorney to determine the starting period, the scope of authorization to carry out business activities.
3, Party A to provide medical devices must meet the following requirements:
(1), the quality of medical devices should be consistent with the national quality standards and production enterprises factory qualified standards and the national functional departments to determine the relevant quality requirements.
(2), medical device instructions, labels, packaging should be consistent with the "medical device instructions, labels and packaging labeling regulations" requirements, and comply with the relevant product transportation, storage requirements.
4, Party A shall provide Party B with medical equipment products responsible for product installation, maintenance, technical training services or Party A to contact a third party to provide technical support. The implementation of the national after-sales products to implement the "three packages" service and commitment to the relevant provisions:
(1) Party A is responsible for the product. Transportation, installation, commissioning and operation training until the product can be used normally and Party B's operators can be skillfully operated.
(2) in the product installation and commissioning, the warranty period found in the process of quality problems, Party A shall be responsible for timely and convenient for Party B customers to replace or return processing, the specific operation of the link by the two sides to determine the negotiation.
(3) in the product warranty period, Party A shall provide the necessary debugging, maintenance and technical services and product "three packages" services within the relevant accessories, the corresponding costs incurred by the two sides to decide by mutual agreement.
(4) After the expiration of the warranty period, Party A shall continue to provide quality service, the supply of spare parts and maintenance costs are determined by mutual agreement.
5, Party A to provide product quality to make the following commitments:
(1) Party A to ensure the legitimacy and authenticity of the information provided, such as the provision of false information and other issues arising from all the adverse consequences of Party A is fully responsible.
Medical Device Quality Assurance Agreement Part 3To ensure the quality of medical devices, to ensure the safety and effectiveness of medical devices. In accordance with the "supervision and management of medical devices regulations" and related laws and regulations, we strictly abide by the laws and regulations to ensure the effectiveness of the product distribution operating procedures, and the quality of medical devices sold to you to make the following commitments:
1, we are engaged in the sale of medical devices with a medical device business license, medical device product registration certificate;
2, we provide the Medical equipment meets the quality standards, all qualified products;
3, we provide medical equipment to provide standardized after-sales service;
4, once we find product quality problems, we will notify you in a timely manner and take appropriate recall and other measures to ensure that the user's interests and safety.
5. This quality guarantee is valid for a long time.
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