All the hospital's medical, teaching, scientific research instruments and equipment required by the equipment section is responsible for procurement, supply distribution, management and maintenance.

Second, according to the requisition plan of each department and the reserve situation, the preparation of the procurement plan, organization and procurement.

Three, general medical supplies according to the plan of the name, specifications, model, the number of procurement, valuable instruments, large precision instruments and equipment, by the technical engineering staff of this section, together with the relevant sections of the analysis of the advanced nature of the purchased instruments, the use of reliability, and the economic and social benefits of the analysis by the Instrumental Management Committee will be reported to the dean for approval after the implementation of the demonstration.

Four, the purchase of instruments, instruments and equipment must fulfill the strict procedures for entry and exit of the warehouse, equipment warehouse according to the nature of the instruments, instruments, classified storage, so that the account matches the goods, the warehouse should be ventilated, moisture-proof, clean, to prevent damage to the instruments.

Fifth, a variety of medical instruments and custody of the request, each department shall be responsible for a person. Purchase of domestic and foreign valuable instruments and equipment, should be technicians and relevant personnel to participate in the acceptance, and then warehousing on the account card, the establishment of technical files, with the relevant departments to develop the use and management system, such as instrumentation found to be problematic, in accordance with the provisions of the procedures for the return of goods, claims, maintenance and so on.

Sixth, the equipment section of the hospital's valuable equipment for regular maintenance and repair of the first level, the departments need to repair the instrumentation, should fill out the application form sent to the equipment section by the maintenance staff to organize maintenance, the establishment of a weekly inspection of the instrumentation system, maintenance staff should be in-depth repair of the department at regular intervals.

Seven, the equipment section should be a year on the hospital's medical equipment, instruments and equipment to carry out a comprehensive inventory, inventory, check, so that the account matches.

Equipment purchase approval system

One, each business unit should be based on clinical, scientific research, teaching needs of the annual preparation of equipment plans, more than 100,000 yuan of equipment should be filled out the plan demonstration form, summarized by the medical equipment management department, to the Medical Equipment Management Committee for discussion, the formation of the annual plan, and approved by the leadership of the hospital after the implementation of

On the second acquisition of large-scale medical equipment, must first prepare a feasibility report and a report on the feasibility of the purchase of medical equipment. equipment, must first prepare a feasibility report and application form for the configuration of large-scale medical equipment, reported to the Provincial Health Department for approval and implementation. (Subject to the documents of the Provincial Department of Health)

Three, the emergency or clinical urgency of the medical equipment, should be used by the department to submit an application to the hospital leadership for approval, priority processing.

Four, the business departments shall not sign a contract of order or commitment to the vendor to purchase intention. Attendance at various meetings, you can bring the product information introduced by the manufacturers at the meeting back to the unit, in accordance with the relevant procedures for approval.

Fifth, the various types of equipment required for the consumables, accessories, should be a good plan by the medical equipment management department for review, reported to the supervisor for approval of the implementation.

Sixth, the medical equipment needed for scientific research projects, should be based on scientific research funding, approval of the project, by the department of science and education to put forward a unified plan, reported to the equipment management department for review and approval of the implementation of the leaders in charge.

Seven, for gifts, scientific cooperation, clinical trial or verification of medical equipment, must be in accordance with the procedures for the relevant procedures, by the equipment and medical management department review, reported to the unit leader approved the implementation. Violation of the provisions of the medical accident or doctor-patient disputes caused by the parties concerned to bear the relevant responsibility.

Equipment procurement management system

I. The equipment management department should be based on the nature of the business of each specialized department and the needs of medical care, teaching and scientific research, according to the content of the approved plan project procurement.

Two, before the acquisition of medical equipment, must check the supplier to provide a copy of the "Medical Device Registration Certificate", "Medical Device Business License", "Medical Device Manufacturer's License" and other documents must be stamped with the official seal of the distribution unit, and verify the authenticity and validity of the documents. No acquisition of unlicensed and shoddy products, strict quality control.

Third, the procurement of medical equipment in a manner approved by the Government Procurement Office. Medical equipment belonging to the government procurement catalog or centralized procurement bidding scope should be entrusted to bidding procurement in accordance with the provisions. For self-bidding, should be open, fair and just.

Four, for the urgent need and due to special circumstances is not suitable for bidding procurement of equipment, can be used to request quotations or directed single-source procurement, but should be reported to the unit leader for approval. The scope of government procurement should be reported to the local government procurement department for approval.

V. The procurement department shall keep abreast of the progress of the procurement plan, and the equipment that is urgently needed by the clinic shall be procured first in order to guarantee the clinical needs.

VI, the use of the department shall not be unauthorized procurement or trial before payment of medical equipment procurement.

Seven, the consequences of violation of the provisions of the relevant personnel will be pursued.

Equipment acceptance management system

All kinds of medical equipment and consumable materials must be purchased in strict accordance with the acceptance procedures, procedures and strict control. Acceptance of qualified before storage. Failure to meet the requirements or quality problems should be returned in a timely manner or exchange claims. General acceptance procedures are: packaging inspection, unpacking acceptance, quantity acceptance, quality acceptance.

Two, acceptance must be timely, especially imported equipment, must master the contract acceptance and claims period, so as to avoid losses due to untimely acceptance.

Three, the acceptance of medical equipment should be used in the department, medical equipment management and manufacturer's representative *** with the participation of the equipment, such as to apply for import commodity inspection, there must be a local commodity inspection department of the commodity inspection personnel. Acceptance of the results must be recorded and signed by all parties involved in the acceptance *** with.

Four, the acceptance of the situation must be recorded in detail and issued acceptance report, strictly according to the contract name, specifications, model, quantity and acceptance of each item. For all the invoices with the contract does not match the situation, should be recorded, so as to negotiate with the manufacturer in a timely manner or reported to the commodity inspection department claims.

Fifth, quality acceptance should be provided by the manufacturer of the technical indicators or according to the bidding documents committed to the technical indicators, functionality and testing methods, item-by-item acceptance. Acceptance of the technical quality of large-scale medical equipment, should be authorized by the provincial health department of the agency. Acceptance results should be recorded in detail and kept as a technical file.

Sixth, for emergency or first aid acquisition of equipment that can not be accepted in accordance with conventional procedures, you can simplify the procedures, or by the first use of the procedures for acceptance afterwards, but must be signed by the person in charge of medical equipment management department agreed.

VII, acceptance of the equipment should be handled by the person in charge of warehousing procedures. Inventory of a single triplicate, a copy of the accountant for accounting vouchers, a copy of the treasury for storage as vouchers, a copy of the procurement department for storage and inspection.

Eight, the violation of the acceptance of the management system resulting in economic losses or medical injuries, should be held responsible for the responsibility of recognizing.

Equipment operation and use of the management system

One, medical equipment must be developed before the use of operating procedures, the use of operating procedures must be operated in accordance with the operating procedures, unfamiliar with the performance of the instrument and do not have a grasp of the operating procedures shall not be turned on.

Second, the establishment of the use of the registration book (card), the boot situation, the use of the situation, the emergence of problems for detailed registration.

Three, the value of more than 100,000 yuan of equipment, should be kept by a person, a person to use, no one can go on the machine. Large instruments and equipment must obtain the Ministry of Health, "large medical equipment application quality certification" before being put into use, the use of personnel must hold "large medical equipment on the staff of the technical qualification certificate" before being able to operate.

Four, the use of medical equipment, medical equipment departments, should designate a person responsible for the management of equipment, including departmental equipment ledger, each unit of equipment, accessories and accessories management, routine maintenance and inspection of equipment. Such as management personnel work transfer, should handle the handover procedures.

Fifth, the operator in the use of medical equipment should not leave the workplace, such as failure should immediately stop, cut off the power supply, and stop using; at the same time, hang a "fault" sign to prevent others from misuse. Overhaul by the technician is responsible for, the operator shall not be disassembled or overhaul; equipment must be removed only after the fault can continue to use.

Sixth, the operator should do a good job in the daily use of maintenance work, keep the equipment clean. After use, should be properly placed in a variety of accessories, can not be lost.

VII, the use of personnel before leaving work should be in accordance with the prescribed order to turn off the machine, and cut off the power supply, water to avoid accidents. Need to work continuously on the equipment, should do a good job of handover.

VIII, large-scale equipment or clinical diagnosis of the impact of equipment, malfunction and shutdown should be reported to the hospital leadership in a timely manner, notify the medical department, clinical departments to stop billing, so as to avoid unnecessary trouble to the patient.

Nine, the use of the department and personnel to carefully care of equipment, shall not be unauthorized operation. If the illegal operation of the equipment caused by man-made liability damage, to immediately report to the leadership of the department and the medical equipment management department, and in accordance with the provisions of the responsible person for the appropriate treatment.

Medical equipment management system

I. According to the medical, teaching, scientific research, the development of preventive work needs, by the use of the department to apply for the compilation of procurement plans, reported to the dean for approval after the implementation.

Second, the general use of medical instruments and equipment, equipment according to the approval of the type, model, the number of organizations to purchase.

Three, large and expensive medical instruments and equipment, must be carried out in a variety of demonstration, by the hospital instrument management will be discussed, and reported to the dean for approval after the implementation.

Four, where the purchase, use of instruments, equipment, must strictly fulfill the acceptance, warehousing, warehousing procedures, make a good account, card, bookkeeping; and do a good job of technical files, with the use of the department to establish operating procedures.

V. Valuable instruments and equipment, the use of the department must be used by a person, a person responsible for the use, maintenance, the establishment of the machine license system. Equipment Section of the regular inspection, maintenance, failure to report timely, the organization to deal with.

VI, the loss of efficacy and do not adapt to the clinical requirements of medical equipment and equipment, in accordance with the provisions of the end-of-life procedures, in order to update the purchase. Idle and low utilization rate, the Equipment Division timely transfer transfer, the use of departmental comments, reported to the dean for approval.

VII, a variety of instruments and equipment in need of repair, should fill out the repair order in a timely manner, the equipment section of the organization maintenance. Maintenance personnel regularly in-depth department, tour maintenance.

Medical instruments and equipment maintenance, maintenance system

I, the use of equipment maintenance applications, maintenance personnel should be timely response and processing. After the maintenance is completed, the maintenance personnel should fill in the maintenance records in detail and notify the using department to resume the use.

Second, on the unsolvable or difficult problems should be reported to the higher leadership in a timely manner.

Three, the first aid equipment, maintenance personnel shall not be delayed for any reason, but should be actively repaired to ensure that the first line of clinical needs.

Four, the use of the department should be in accordance with the provisions of the daily maintenance of medical equipment, and regularly check the implementation of the implementation of the situation.

Fifth, the regular deep-rooted section of the instrumentation and equipment responsible for safety inspections, timely detection of problems and timely treatment to prevent accidents.

VI, actively create conditions for preventive maintenance (pm maintenance), reduce the probability of equipment failure.

Seven, the warranty period or the acquisition of warranty contracts for the equipment, to master its use. Problems arise, in a timely manner with the warranty factory contact, the results of the maintenance of the corresponding maintenance records, and check the implementation of the warranty contract.

Eight, should do a good job during breaks and holidays maintenance duty, to ensure that holidays and breaks are able to deal with unexpected maintenance requirements.

nine, to maintain the safety and cleanliness of the work area. Keep a variety of maintenance tools, instruments, to prevent loss and damage.

Ten, regular business meetings, at least once a month to organize business learning, research, analysis and maintenance of difficult problems, exchange of maintenance experience.

Equipment transfer management system

Which meets one of the following conditions can be transferred to deal with:

A cumulative total of more than one year out of service idle equipment. Belong to the spare, maintenance, technical transformation, special reserves and disaster relief equipment except.

Second, due to changes in the work no longer use the equipment: technical indicators have declined, but has not reached the end of the standard can still be degraded to use the instrumentation; repeated acquisition of the same instrumentation, the average utilization rate of less than 20%.

Three, it is strictly prohibited to the relevant state departments expressly prohibit the production, elimination, proliferation and transfer of medical equipment or equipment to be scrapped as idle equipment transfer.

Four, the transfer of equipment for domestic use, the approval of the approval should be strictly approved and check.

Fifth, the transfer of equipment should be based on the principle of the nearest within the transfer, try to avoid long-distance transportation, resulting in unnecessary losses.

Sixth, all transfers of equipment, including gratuitous transfer of medical equipment, in the valuation, should be based on the use of the period, the state of the technology and other reasonable price, the two sides negotiated and signed an agreement, according to the contract.

VII, the actual handling of the financial procedures to be carried out in a timely manner, the transfer of receipts should be listed in the equipment renewal, renovation of the fund project for special use, shall not be diverted to other purposes.

VIII, all the equipment to be transferred, should be in accordance with the provisions of the equipment management department for proper storage and sealing, shall not be arbitrarily disassembled to prevent corrosion, damage, loss.

Nine, strengthen the financial management and supervision of the transfer of equipment, the use of transfer of equipment to facilitate the loss of public funds for personal gain should be pursued and seriously dealt with.

Medical equipment scrapping and reporting system

I, where medical equipment in line with the conditions of end-of-life can not be used for clinical use, should be scrapped.

Second, the application for scrapping of medical equipment, should be proposed by the use of the department; by the equipment management department register, fill out the "scrapping of medical equipment application form"; by the relevant technical departments to carry out technical appraisal; equipment supervisor to put forward the transfer of scrapping opinions; the financial sector to handle the relevant procedures.

Three, more than 10,000 yuan of medical equipment scrapped, according to the state-owned assets at all levels of government administration of the state-owned assets disposal of administrative institutions management implementation of the "procedures for reporting.

Four, where tax exemption imported medical equipment bottom according to the above provisions should also be handled in accordance with the relevant provisions of the Customs. For the disposal of equipment available for domestic use, should strengthen the audit, strict control.

Fifth, to be scrapped medical equipment should be properly stored before approval, has been approved for the scrapping of large-scale medical equipment should be used to remove part of the discounted value of the people in storage, reasonable use.

Sixth, approved by the end of the medical equipment, the use of units and individuals shall not be disposed of on their own, are returned to the equipment department for unified treatment. If the violators should be traced and handed over to the competent authorities.

VII, has been approved by the end-of-life medical equipment in the treatment, should be timely for the financial write-off procedures, the residual value of the proceeds should be listed in the medical equipment renewal fee, transformation fund project special use.

Medical equipment damage incident handling system

I, all types of medical equipment damage occurs, the relevant personnel should immediately report to the medical equipment management department, and truthfully respond to the situation, shall not be pushed to the Japanese, concealment and non-reporting.

Second, in accordance with the rules of operation, man-made damage caused by less than ten thousand yuan of medical equipment, but can still be repaired but does not affect the use of the general accident.

Three, due to the failure to operate according to the procedures, man-made damage caused by less than ten thousand yuan of medical equipment and can not be repaired, according to the responsibility of the accident. Compensation costs are determined according to the use of life depreciation.

Four, due to poor work responsibility, negligence, resulting in more than ten thousand yuan of medical equipment damage and can not be repaired, according to the major liability accident. Medical equipment management committee in the study of the responsible person to put forward treatment opinions, reported to the hospital leadership for approval. Compensation costs are determined after depreciation according to the service life.

Fifth, medical equipment and low value consumables due to mismanagement of the lost, according to the original price of compensation; damage caused by the damage should be determined according to the degree of compensation costs.

Sixth, medical equipment damage occurs, always by the maintenance staff to repair. Without consent to repair damage caused by the responsible person by the original value of medical equipment depreciation and compensation.

Measuring instruments management system

I. Measuring instruments management system

(a), belonging to the mandatory testing of measuring instruments should be a person (measurement administrator) is responsible for the management and coordination.

(2), under the supervision and guidance of the higher measurement department, the hospital measurement committee and medical equipment management department in accordance with the requirements of the "Measurement Law" and the relevant provisions of the unified management of the hospital's measurement work.

(3), the unified establishment of the hospital's mandatory verification of measuring instruments account, sub-accounts, ledgers, and keep the relevant technical files and certificates of verification.

(d), to strengthen business contacts with the measurement and verification departments to do a good job of the annual cycle of mandatory calibration of measuring instruments.

(E), randomly on the use of measuring instruments for sampling, to stop the use of overdue or unqualified measuring instruments.

(F) the consequences of violations of the measurement system, reported to the leadership for appropriate treatment.

Two, the purchase of measuring instruments, storage, degradation and loss reporting system

(a), the acquisition, to review the model of measuring instruments, specifications, precision level, measurement range, measurement performance, in order to ensure that the measurement of the performance of accurate and reliable.

(ii), the purchase of measuring instruments should be cmc or cpa logo (with license number), shall not purchase measuring instruments produced by enterprises that have not obtained a license to manufacture measuring instruments.

(3), measuring instruments purchased, should keep the relevant technical information, before use should be sent to the measurement of the measuring instruments measured by the department.

(d), acceptance and verification of qualified measuring instruments before the library, while the measurement of the administrator to establish an account and prepare a regular verification program.

(E), the acceptance or verification of unqualified measuring instruments, by the equipment section of the report on the return of the original procurement department for the return.

(F), measuring instruments by the test can not reach the original accuracy level, but can achieve a lower level of accuracy, can be used for downgrading, and make a good change in the technical file records.

(vii), by the test failed and repair still can not pass the test of measuring instruments, measured by the administrator of the end-of-life report, by the medical equipment management department to deal with.

Three, the use of measuring instruments, maintenance, maintenance system

(a), the use of measuring instruments, the department must do a good job in the use of measuring instruments and maintenance work, the development of the corresponding use of operating procedures, by a person responsible for, and in strict accordance with the instructions and operating procedures.

(ii), all measuring instruments should establish the use of records and regular maintenance and repair; commonly used measuring instruments should be wiped clean after each use of maintenance, infrequently used should be done on a regular basis power test.

(3), the place of storage measuring instruments, clean and sanitary requirements. Temperature, humidity to comply with the provisions of the verification procedures, and maintain relative stability. Easy to deform the measuring instruments, to be categorized and stored properly. Strictly prohibit measuring instruments and acids, alkalis and other corrosive substances and abrasives mixed.

(d), in use measuring instruments must be measured identification certificate or qualified mark, found that the certificate of conformity is lost or overdue, we must promptly find the reasons for the replacement procedures.

(E), measuring instruments failures should be reported to the measurement of the administrator in a timely manner, the use of the department does not have the right to unauthorized repair of measuring instruments. Precise and valuable instruments approved by the competent leader to send repair, and make a record.

(F), one of the following cases of measuring instruments shall not be used: unqualified or unqualified test; more than the test cycle; no valid certificate or seal; measuring instruments in the effective use of the period of inaccuracy, malfunctioning; without the approval of the government administrative department of measurement of non-statutory units of measurement instruments; the unit can not be repaired measuring instruments should be entrusted to obtain a "repair of measuring instruments license

Four, measurement of documents, technical files and information management system

(a), measurement of documents, technical information, quality vouchers, documents to be kept by a person and numbered, registration, loaned to fulfill the loan procedures to prevent loss and damage.

(2), carefully fill out the measurement of technical files, so that the content is complete, the handwriting is correct, in line with the relevant norms of the national measurement department.

(C), according to the prescribed retention time to keep measuring documents and technical files, if the destruction of archival materials subject to approval.

(d), the occurrence of loss of measurement of the file should be well documented, to find out the reasons and then held accountable.

V. Measurement of accident management

In the medical process, may be due to the accuracy of medical measuring instruments or other measurement problems caused by medical disputes or medical accidents. If such problems occur, can be dealt with in the following ways:

(a), the way to deal with measurement disputes have been inspected and mediation, first of all, we must find out the facts, right and wrong, clear responsibility, based on mutual understanding to promote mutual understanding between the parties to solve the problem.

(2), measurement of mediation is by the county level above the Technical Supervision Bureau of the measurement of disputes between the two sides of the mediation. According to the special circumstances of measurement disputes, measurement of mediation should generally be carried out after the arbitration test.

(3), the arbitration test is referred to by the county level or above, the Technical Supervision Bureau with the measurement of benchmarks or social measurement standards for the purpose of arbitration measurement test, testing activities. Arbitration test can be directly accepted by the county level above the Bureau of Technical Supervision, or to designate a qualified measurement and testing organization.

(4), the circumstances are serious and cause medical accidents, the scene should be protected so that the relevant personnel to come to find out the cause of the accident and record; in accordance with the relevant laws of the country.

(5), general accidents caused by human factors, should be given to the parties involved in the appropriate treatment; if caused by mismanagement, should analyze the causes and develop appropriate management system to avoid the recurrence of similar events.

Information file management system

I. According to the provisions of the Archives Law, according to the level of management of medical equipment, to determine the establishment of the scope of medical equipment file management.

Second, the archives should be carefully filled out in accordance with the provisions of the project content, so that the handwriting is correct, complete, clear and categorized and numbered registration. Data collection should be true and complete. File catalog should be consistent with the contents of the file.

Three, improve the technical file borrowing procedures. Large precision instruments of the original technical files, non-approved shall not be borrowed. Medical equipment instruction manual copy or copy to the use of the department.

Four, technical files should be stored in accordance with the prescribed retention time, the destruction of files, information to be approved.

V. Do a good job in a timely manner to update the dynamic file information.

VI, to ensure that the information management system data security, regular backup data.

VII, file managers work changes, according to procedures for file transfer procedures.

Professional equipment bidding management regulations

In order to introduce a fair, just and open mechanism in the procurement process of hospital equipment, based on the "Chinese People's Republic of China *** and the State Bidding Law", the State Development Planning Commission, "Interim Provisions on the Bid Evaluation Committee and Bid Evaluation Methods," the Foreign Trade and Economic Cooperation Commission Decree No. 7, "the implementation of the international tenders for electromechanical products," and the People's Government of Zhejiang Province 96 Decree No. 96 of the People's Government of Zhejiang Province, "Zhejiang Province, mechanical and electrical equipment bidding management approach" provisions, combined with the actual situation of the hospital to develop this provision.

I. Scope of the tender: These provisions apply to the hospital within all single declared value or batch of total declared value of more than 100,000 yuan of professional equipment bidding procurement activities, hospital equipment refers to the equipment section is responsible for the purchase of instruments and equipment used for clinical, teaching, research.

Two, bidding steps: professional equipment bidding procurement is divided into six steps:

(a), the application department in accordance with the relevant provisions of the hospital declaration, project, approval.

(2), the dean in charge, equipment, reporting or use of the department of each supplier's products for demonstration, evaluation, to determine the bidding requirements and configuration of the program, subject to evaluation of the supplier must be more than two.

(3), the equipment section more than a week in advance to the supplier to announce the bidding requirements, bidding time, place and method.

(d), the suppliers in accordance with the requirements of the third point above to make a substantive response.

(5), the dean in charge, equipment, declaration or use of the department, the hospital discipline inspection department *** with the evaluation of the bid to determine the winning unit, to participate in the bidding of the supplier must be more than two, the evaluation method in accordance with the provisions of the national law listed in the first article of the relevant provisions of the implementation of the bidding method.

(6), professional equipment in the consumable materials attached to the part of the bid evaluation team to consult with the Department of Procurement to decide.

The following cases are not included in the bidding and purchasing:

(1) specific accessories and consumables for professional equipment

(2) maintenance parts for professional equipment

(3) exclusive equipment

(4) equipment for which the hospital has entered into a separate agreement

(5) maintenance of equipment and other after-sales service

(6) the evaluation team will consult with the General Procurement Department to decide on the part of consumable materials attached to the professional equipment. After-sales service

(F), according to the state and the Zhejiang Province, included in the bidding catalog of professional equipment

(G), has been entrusted to the bidding intermediary or government procurement office procurement of equipment

(H), does not qualify for bidding of other equipment

4, other matters:

(A), the hospital equipment section is responsible for preserving the tender bidding Information, drafting the minutes of the validation meeting, bidding meeting, and issued by the dean in charge.

(2), the supplier has won the bid in the specified time does not sign the agreement or not to implement the signed agreement, by the equipment section to suspend its bidding qualifications.

(c), the supplier has won the tender to change the bidding requirements or the content of the agreement, in the case does not involve the substantive terms of the equipment section and the use of the reporting department to determine the consultation.

(4), the provisions of the Hospital Equipment Division to develop and is responsible for the interpretation.

Valuable instruments (equipment) use Note

I. The operator must have a high degree of professionalism, sense of responsibility, depending on the instrument as their lives.

Second, must strictly abide by the instrument (operating manual) provided by the operating procedures.

Three, must record the instrument (equipment) use every day, and do a good job of diary work.

Four, the instrument (equipment) must be implemented exclusively for the machine, and strictly do a good job of handover.

Fifth, the instrument (equipment) abnormalities, must immediately stop using, and make a good report, do a good job of recording.

Sixth, the operator must strictly do a good job of routine maintenance, and closely observe the conditions of use.

Seven, in principle, advanced training personnel shall not use the instrument (equipment), in special circumstances, the instructor must strictly supervise, and take full responsibility.

VIII, the operator must do a good job of all safety.

Nine, with the microcomputer configuration of the instrument (equipment), shall not run the machine has nothing to do with the software, or will be traced to the parties involved and the head of the department responsible.

Ten, without the permission of the hospital office, valuable instruments shall not be used without permission from the hospital.

Xi, the use of the instrument (equipment) custody, the head of the department is the first responsible person.