Blood ESR dynamic analyzer is a kind of used to measure the red blood cells sedimentation rate of medical devices, is the hospital and the laboratory commonly used medical apparatus and instruments. Through testing the red blood cells sedimentation rate can be determined, and various kinds of inflammation and necrosis tissue damage, malignant tumor and all causes of high globulin hematic disease, anemia, and high cholesterol disease and so on major body backlog disease, it is very important physical examination indexes.
Because of the important role of blood sedimentation dynamic analyzer, domestic blood sedimentation dynamic analyzer enterprise also is developing vigorously, become a mature industry chain. Blood sedimentation instrument which brand quality is better? Perlong medical is a good choice!
Perlong medical treatment is one has the 19 years history of professionalmedical equipment company, under a variety of many kinds of medical equipment and myocardial products. Perlong medical instrument is also the blood sedimentation market share is very high of medical devices, in all hospitals and laboratories are very popular.
This one blood ESR  dynamic analyzer features it has choice environment temperature compensation function. When choosing the function can be 18 ℃-at 30 ℃ testing results according to correction table correction to 18 blood sedimentation ℃ of value, to ensure the accuracy of the measurement results.

If you to this one blood sedimentation dynamic analyzer and more questions, please click on the right of the page “point I consultation” counseling online customer service, or call our free consultation, please call 400-6656 888-welcome you the arrival!
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Medical equipment industry development in the past two years the hot, many local governments have stepped up the field support, hope that through the spring breeze of the cure of the local medical equipment industry developed. Recently, from the administration’s kunming have learned, only the first half of this year of kunming issued registration certificates 45 class I medical devices, of which the first registered a newly registered, 44.

This data is quite gratifying, compared to previous years had the very big enhancement. Such registration review is very strict, first registered variety classification accuracy, registration data is true and effective, and all varieties through the registered inspection. Medical device registration check, is to ensure that the authenticity of the enterprise application material, avoid fraudulent false declaration of important regulatory means. In accordance with the relevant documents GuoGuJu factories in kunming regulations, implement medical device registration for verification. Focus on whether the existing medical equipment according to medical equipment is declared or high class low cross;

The kind of medical device manufacturing enterprise registration form “, whether they contain the variety; Ensure that the main body of the administrative licensing legal; Directly used to gb and line mark, or the enterprise standard (registered product standards) cited corresponding mandatory national standard and professional standard is no current effective; Key check whether a enterprise performance test all the test conditions; Entrusted by the inspection of, whether to have entrusted inspection agreement, be entrusted inspection institutions have inspection conditions; The enterprise existing resources and quality management ability (including detection means)
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With prosess of medical reform, medical devices began to become popular.Many investors turn their attention to this area,medical equipment is emerging up the industry for expertise in a lot of investors are not very understanding of this invisibleto invest a certain amount of risk. Below are we encountered a problem and solution.

23.What is role Clinical medical staff play in the medical device adverse events inspection?

As a medical device adverse events (one of the main body of report, a medical institution is most the use of medical equipment room, also be the main medical device adverse events occurred. At the same time, as a medical institution staff, clinical medical staff has professional background and industry position, can grasp the event first-hand material, and it has good ability to identify. Therefore, clinical and medical personnel in the medical device adverse event monitoring play an important role. Medical personnel to report, analysis medical device adverse events, with enterprise and related departments of the survey, is to make sure the public safety with an important guarantee of soldiers.

24 What is the re-evaluation of medical devices?

Medical equipment re-evaluation refers to safety of medical devices approved for marketing.The effectiveness of re-evaluation, and implementation of corresponding measures of process.

25.What is the function of medical equipment manufacturer in medical devices re-evaluation ?

Medical device manufacturing enterprise is the main body of medical equipment and evaluation, should according to medical equipment product technical structure, quality system requirements set medical equipment to start conditions, evaluation program evaluation and the method; According to carry out the conclusion to evaluation shall, when necessary, be according to relevant provisions of his medical device registration registration procedure.

26 What is the function of the drug regulatory department in medical devices re-evaluation?

The State Food and Drug Administration and provinces, autonomous regions and municipalities food and drug supervision and management department is responsible for overseeing the re-evaluation to check the medical device manufacturer, if necessary, the organization to carry out the re-evaluation of medical devices.

27. What is medical equipment recovery?

Medical equipment recovery. It is to show medical device manufacturing enterprise in accordance with the procedures prescribed by already listed sales of unsafe products, according to procedures prescribed by the take warning, checked, repaired, the new labels, amend the description, software upgrade, replaced, and withdraw, destroyed, eliminate the product of the harm of way behavior. The recovery includes production enterprise voluntary recall and supervision and management departments.

For medical equipment management, governments around the world are introduced the corresponding measures, to regulate the local medical equipment production and distribution, avoid the happening of the corruption and shoddy medical equipment products into the market, on people’s life security threats. Recent GanYuXian jiangsu province (medical equipment) adverse drug reaction monitoring expert committee officially established.

According to the report by the committee GanYuXian food and drug supervision bureau, health bureau jointly established by the county food and drug supervision bureau of the committee, director of the main person in charge. The county medical institutions engaged in the clinical experts and clinical pharmaceutical research experts 11 people for the committee. Experts committee will exert their professional technical force and rich clinical experience, to the county regularly drugs, medical devices and adverse reaction of new, serious adverse reactions (events), the organization carries out the analysis and evaluation of the death of investigation, evaluation, judgment, of the national requirements of adverse drug reaction monitoring varieties key for monitoring and evaluating analysis.

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The annual college entrance examination is over, now has come to fill the key moment of the volunteer, each students studying in when the choice is professional is also very careful, because it is possible that this is the relationship between a lifetime of things.Recently on the higher school year announced the 2011 professional setting record or examination and approval of the “notice of shows, henan province university in 2012, 141 new professional, including four professional new xinxiang medical school, respectively is psychology professional, medical equipment engineering, health inspection professional and marketing professional. According to the Chinese education online understanding, xinxiang medical school plan recruit students this year to 3310 people, among them, the number of new medical equipment engineering plan recruit students 30 people in henan province.

Through the college expansion, we found that, in recent years the rapid development of the medical devices field talent or scarce, and medical equipment technology in progress is a lack of professionals. Xinxiang medical school, the number of new medical equipment engineering (4-medical-year) for science class is to cultivate the engaged in medical instrument equipment operation, use, maintenance and repair and understanding. Modern clinical medical instrument development with the compound engineering technology. According to information, medical equipment engineering graduates employment mainly to the hospital, in the first line of clinical medical personnel engaged in medical equipment with the operation maintenance, management and maintenance work, especially the human body is directly related to the life of the human body function auxiliary devices and monitoring devices, such as breathing machine, a heart-lung machine, blood dialysis machines and eloquence monitoring equipment, etc, to ensure that equipment in clinical use of safety and effectiveness, also can be in Chinese and foreign enterprises and institutions for medical devices in the development of the product, manufacturing, marketing and management.

Henan xinxiang medical school is province-owned higher school undergraduate course, is located in the coast of the Yellow River, the foothills mountain in shansi makino city–the xinxiang city. Institute was founded in the late nineteenth century, in May 1950, the formal school, formerly known as plain province medical school. In September 1962, renamed north medical college. In November 1982, the school upgraded to degree, and name for xinxiang medical school. In June 1998, the state council approved by the academic degrees committee, become a master’s degree awarding units. Since since school, the school already cultivate medical personnel 40000 more than person.
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Wednesday, January 11, 2012
AACC ANNOUNCES 2012 OAK RIDGE CONFERENCE
Washington, DC, January 11, 2012

The American Association for Clinical Chemistry (AACC) announces its 2012 Oak Ridge Conference: Emerging Technologies for 21st Century Clinical Diagnostics to be held April 19 – 20, 2012, at The Fairmont in San José, CA.

Come to Los Angeles in 2012 to visit even more exhibitors in more booths than ever before. In addition, you will see more products in every clinical lab discipline than at any other show. We expect greater than 650 exhibitors occupying more than 1,900 booths.

Also,Many China Medical Equipment get well preparation for AACC2012 Meeting.Most leading Equipments & Technologies for Medical and Surgery Trade Shows in AACC2012 Meeting.Among various manufacturer,Perlong Medical devote their great efforts to improve Medical Equipment Technology.
As one of China leading medical equipment manufacturer,Perlong Medical hold positive preparations for AACC2012.We will display our key products,high frequency x ray machine,Reformed Blood Analyzer,also with some new equipment with advanced Technology.Welcome to meet us in AACC2012.We are happy to serve you.