Tuesday, June 3, 2014

National indépendante technologie d’échographie à briser la barrière de traitement de la prostate.

Prostatite et l'hyperplasie prostatique sont principal maladies de la prostate,appelée "le tueur" de santé des hommes.La prostatite est plus fréquente chez les jeunes hommes,et l'hyperplasie bénigne de la prostate est une maladie courante chez les hommes âgés.La prostate est un organe important du système génito-urinaire mâle,situé au fond du bassin,garde urètre ci-dessus,elle a de trou communique avec le canal déférent.Prostatite et l'hyperplasie prostatique sont lès principal les maladies de la prostate,appelée «tueur» de la santé des hommes.La prostatite est plus fréquente chez les jeunes hommes, et l'hyperplasie bénigne de la prostate est une maladie courante chez les hommes âgés,plus de la moitié des hommes de 60 ans ont des degrés différents de symptômes de l'hyperplasie.Pendant longtemps,la membrane que enveloppé a l'extérieur de prostate,Comme une barrière dur,ça fait toutes sortes de médicament traitement des maladies de la prostate ne peuvent pas pénétrer,par conséquent, l'effet est fortement diminué.Avec le développement de la technologie médicale,la technologie des ultrasons (cheap ultrasound machine) a finalement brisé cette couche barrière,Effets du traitement de la maladie de la prostate a radicalement changé. 
desktop human ultrasound body scanner 
Selon les rapports,l'échographie en médecine est une discipline émergente,Instituts nationaux de santé NIH,le première institut qui essaie la technologie des ultrasons (veterinary ultrasound) utilisés dans le traitement des maladies,avec l'Université de Harvard composite institutions de recherche coopérative a investi massivement dans le développement d'une coalition a développé américaine INNOVAX séries dispositif de traitement à domicile,le produit balayé rapidement en Europe et en Amérique. En Chine,Groupe de travail de 20 experts,qui viennent des Guochuang Tech biomédicale Engineering Co., Ltd.et Pékin Chong Tech Institut de génie biomédical,Chine Institut de génie biomédical clinique ont passé une décennie,en utilisant la technologie puce et l'échographie nanotechnologie numérique intégré a prostate de américaine INNOVAX,développé avec succès une matériel médical d'accueil qui avec des droits de propriété intellectuelle quasi-célèbre,pour apporter l'évangile de patients atteints de maladies de la prostate. 
Il est rapporté que la technique utilise la capacité de pénétration du ultrason ,pénétre la prostate non-invasive dans le profondeur 100-120 mm profondeur,attaque lésions zéro à distance et fortement.résout ce problème que médicament est difficile à pénétrer la capsule de la prostate complètement.Sous la direction de l'échographie, drogue entre la glande sans difficulté.Pendant ce temps,l'haute technologie silver Nano de pâte de guidage sonore pour traitement,a la fonction de perméabilité supérieure,peut tuer une variété de bactéries spécifiques, les germes et les microbes tenaces puissant.À double effet par ultrasons (wrist ultrasound) et médicament plus à fond pour tuer les bactéries, éliminer l'inflammation, l'effet thérapeutique peut être renforcée.De plus, les ultrasons a également une fonction de massage,1,7 million de fois par seconde vibrations denses des tissus,ça fait le métabolique de la glande bien dégagé rapidement,alors que la vibration à grande vitesse peut également produire cinq fois la température de surface de la chaleur.Dans le même temps à tuer les bactéries dans la glande, de sorte que le flux d'adoucir glandulaire, améliorer l'approvisionnement en sang. 
Il est rapporté que ce produits high-tech ont entrés sur le marché à Chengdu . 
The article comes from: http://www.medicalequipment-msl.com/fr/htm/livre-de-dispositif-m%C3%A9dical/National-ind%C3%A9pendante-technologie-d%C3%A9chographie-%C3%A0-briser-la-barri%C3%A8re-de-traitement-de-la-prostate.html 
Related Posts 
Medical ultrasonography 
China's first Full Digital Color Doppler ultrasonic Diagnostic instrument Officially available.

National indépendante technologie d’échographie à briser la barrière de traitement de la prostate.

Prostatite et l'hyperplasie prostatique sont principal maladies de la prostate,appelée "le tueur" de santé des hommes.La prostatite est plus fréquente chez les jeunes hommes,et l'hyperplasie bénigne de la prostate est une maladie courante chez les hommes âgés.La prostate est un organe important du système génito-urinaire mâle,situé au fond du bassin,garde urètre ci-dessus,elle a de trou communique avec le canal déférent.Prostatite et l'hyperplasie prostatique sont lès principal les maladies de la prostate,appelée «tueur» de la santé des hommes.La prostatite est plus fréquente chez les jeunes hommes, et l'hyperplasie bénigne de la prostate est une maladie courante chez les hommes âgés,plus de la moitié des hommes de 60 ans ont des degrés différents de symptômes de l'hyperplasie.Pendant longtemps,la membrane que enveloppé a l'extérieur de prostate,Comme une barrière dur,ça fait toutes sortes de médicament traitement des maladies de la prostate ne peuvent pas pénétrer,par conséquent, l'effet est fortement diminué.Avec le développement de la technologie médicale,la technologie des ultrasons (cheap ultrasound machine) a finalement brisé cette couche barrière,Effets du traitement de la maladie de la prostate a radicalement changé. 
desktop human ultrasound body scanner 
Selon les rapports,l'échographie en médecine est une discipline émergente,Instituts nationaux de santé NIH,le première institut qui essaie la technologie des ultrasons (veterinary ultrasound) utilisés dans le traitement des maladies,avec l'Université de Harvard composite institutions de recherche coopérative a investi massivement dans le développement d'une coalition a développé américaine INNOVAX séries dispositif de traitement à domicile,le produit balayé rapidement en Europe et en Amérique. En Chine,Groupe de travail de 20 experts,qui viennent des Guochuang Tech biomédicale Engineering Co., Ltd.et Pékin Chong Tech Institut de génie biomédical,Chine Institut de génie biomédical clinique ont passé une décennie,en utilisant la technologie puce et l'échographie nanotechnologie numérique intégré a prostate de américaine INNOVAX,développé avec succès une matériel médical d'accueil qui avec des droits de propriété intellectuelle quasi-célèbre,pour apporter l'évangile de patients atteints de maladies de la prostate. 
Il est rapporté que la technique utilise la capacité de pénétration du ultrason ,pénétre la prostate non-invasive dans le profondeur 100-120 mm profondeur,attaque lésions zéro à distance et fortement.résout ce problème que médicament est difficile à pénétrer la capsule de la prostate complètement.Sous la direction de l'échographie, drogue entre la glande sans difficulté.Pendant ce temps,l'haute technologie silver Nano de pâte de guidage sonore pour traitement,a la fonction de perméabilité supérieure,peut tuer une variété de bactéries spécifiques, les germes et les microbes tenaces puissant.À double effet par ultrasons (wrist ultrasound) et médicament plus à fond pour tuer les bactéries, éliminer l'inflammation, l'effet thérapeutique peut être renforcée.De plus, les ultrasons a également une fonction de massage,1,7 million de fois par seconde vibrations denses des tissus,ça fait le métabolique de la glande bien dégagé rapidement,alors que la vibration à grande vitesse peut également produire cinq fois la température de surface de la chaleur.Dans le même temps à tuer les bactéries dans la glande, de sorte que le flux d'adoucir glandulaire, améliorer l'approvisionnement en sang. 
Il est rapporté que ce produits high-tech ont entrés sur le marché à Chengdu . 
The article comes from: http://www.medicalequipment-msl.com/fr/htm/livre-de-dispositif-m%C3%A9dical/National-ind%C3%A9pendante-technologie-d%C3%A9chographie-%C3%A0-briser-la-barri%C3%A8re-de-traitement-de-la-prostate.html 
Related Posts 
Medical ultrasonography 
China's first Full Digital Color Doppler ultrasonic Diagnostic instrument Officially available.

Wednesday, May 28, 2014

Who will bear the responsibility for security of medical devices


Whether the medical equipment of the hospital safe? Who is responsible for the problem ? How to safeguard rights when the accident happen? 
The newly revised"Medical Devices Regulations"established the most stringent regulatory system covering the whole process.And long before the"Regulations" release,the State Food and Drug Administration has already begun work on rectifying the cheap lead glasses medical device industry.From mid-March,for a period of five months of medical devices"Five remediation"special action,carried out in the country,focusing on regulation of medical devices registered false reporting,illegal production and illegal business,hype,the use of unlicensed products and so on. 
Sampling,strong inspection can not be guaranteed,it lay hidden for safety Worked in the medical device industry more than ten years Mr.Xu believes that lack sophisticated technology medical device industry,the overall industrial backwardness,is an important cause of domestic medical equipment industry worse than abroad.But in Chinese Medicine Association of Medical Device Materials Branch Secretary Chen Hongyan seems that the threshold is too low,lax supervision,lazy Responsibility chaos as a result of the medical device industry is currently facing the biggest problem. 
veterinary ultrasound 
Under the existing regulations,all medical device companies need to apply to the competent agency for"Medical Device Manufacturing Enterprise License"before you can apply for production licenses in the local business sector.Before the products get out the factory,this should be carried out in the factory in the inspection,sampling and accept the country,after the quality standards in order to enter the hands of the operators,by their products to sales terminals.However,some small businesses ignore internal inspection,sampling escaped the country after he met the acceptance lax operators,it will lead to poor quality products all the way to the green,to the market. Director of Department of Peking University People's Hospital Equipment Shen Chen Yang told reporters,when the device enters into the use of medical institutions,belongs to the state measurement detection range must undergo a compulsory annual measuring and testing to ensure its quality.However,Mr.Xu said that in some grassroots small hospital,because of poor management,can not guarantee strong inspection once a year,causing a problem of extended service of medical devices,planted health risks to users. 
Medical institutions,strong sense of responsibility for the patient to recover "Although the quality of medical equipment,related to the life and health,but in the rights,whether institutions or the people themselves,are not strong enough sense of Responsibility."For example,you bought a home therapy device,found the problem to find manufacturers,manufacturers may apart from anything else and then replace it give you,you would not bother to chase a responsibility;If you buy a mask,Band-Aid kind of low- value products,if found good,that is most readily throw away,even the manufacturers are not look for.In the medical institutions,large hospitals simply do not survive inferior equipment,and small organizations to buy quality if there are problems,that is,directly to the manufacturer for repair or replacement.Events occur as long as there is no real threat to the life,inferior products will be able to muddle through,the manufacturer will be able to avoid liability. 
It is understood that after the implementation of the"Medical Devices Regulations"issued in 2000,10 years,with the development and changes in China's medical equipment industry,which is not suitable for development of the industry situation even more prominent.For example,it is responsible for the chase would not provide details on the terms of the lack of bad product traceability system. 
The newly revised"Supervision and Regulation of Medical Devices"provides medical equipment enterprises,and use of medical equipment purchased should pass inspection documents the supplier qualification and medical equipment,establish inspection record system.The second class,third class medical equipment wholesale business as well as Class III medical devices retail business ventures,sales records system should also be established.Medical equipment unit shall keep the original data acquired Class III medical devices,and to ensure that the information traceability. 
No matter what the problem is now in the presence of the medical device market,the new draft amendments are introduced to the industry on a"safety valve",the management of medical devices and drug control in the same position.Of course,the law,also need to be strictly enforced to ensure excellent products,anesthesia ventilator industry health. Production will be the focus of regulation violations 
With the launch of the special action,the medical device industry consolidation horn sounded.The official said that for a false registration application behavior,the second will focus on remediation,Class III medical devices registration untrue behavior for the first time,carried out in accordance with the provisions of the second,three types of medical equipment for the first time to submit an application for registration of producers of information (focus is on clinical trials report) and verification of the authenticity of tissue samples of the production process,the registration link in the report focus on verification. 
Production is also a violation of content regulation.Disposable infusion equipment,single-use catheters (package) does not meet the criteria for raw materials and did not seek sterilization,condoms without filing unauthorized commissioned production,hemodialysis concentrates not according to the standard factory inspection,etc.,will be the focus of regulation. 
In the circulation,illegal operation and will be glued to commence remediation hype behavior.For example,experiential approach to unauthorized sales of the second,three types of medical equipment,unlicensed plain lead eyewear colored decorative contact lenses,hearing aids,did not seek storage and transport in vitro diagnostic reagents and other acts.Again,back pain,myopia,diabetes and hypertension sticking classes,physical therapy medical devices for illegal propaganda;without the approval or approval of the content of tampering unauthorized release illegal advertising,exaggerating the effectiveness and scope of the product;use of medical research institutes or specialists,patient name and image to do to prove the efficacy of advertising and other unlawful acts,etc.. 
The article comes from:http://www.medicalequipment-msl.com/htm/medical-device-book/Who-will-bear-the-responsibility-for-security-of-medical-devices.html

Who will bear the responsibility for security of medical devices


Whether the medical equipment of the hospital safe? Who is responsible for the problem ? How to safeguard rights when the accident happen? 
The newly revised"Medical Devices Regulations"established the most stringent regulatory system covering the whole process.And long before the"Regulations" release,the State Food and Drug Administration has already begun work on rectifying the cheap lead glasses medical device industry.From mid-March,for a period of five months of medical devices"Five remediation"special action,carried out in the country,focusing on regulation of medical devices registered false reporting,illegal production and illegal business,hype,the use of unlicensed products and so on. 
Sampling,strong inspection can not be guaranteed,it lay hidden for safety Worked in the medical device industry more than ten years Mr.Xu believes that lack sophisticated technology medical device industry,the overall industrial backwardness,is an important cause of domestic medical equipment industry worse than abroad.But in Chinese Medicine Association of Medical Device Materials Branch Secretary Chen Hongyan seems that the threshold is too low,lax supervision,lazy Responsibility chaos as a result of the medical device industry is currently facing the biggest problem. 
veterinary ultrasound 
Under the existing regulations,all medical device companies need to apply to the competent agency for"Medical Device Manufacturing Enterprise License"before you can apply for production licenses in the local business sector.Before the products get out the factory,this should be carried out in the factory in the inspection,sampling and accept the country,after the quality standards in order to enter the hands of the operators,by their products to sales terminals.However,some small businesses ignore internal inspection,sampling escaped the country after he met the acceptance lax operators,it will lead to poor quality products all the way to the green,to the market. Director of Department of Peking University People's Hospital Equipment Shen Chen Yang told reporters,when the device enters into the use of medical institutions,belongs to the state measurement detection range must undergo a compulsory annual measuring and testing to ensure its quality.However,Mr.Xu said that in some grassroots small hospital,because of poor management,can not guarantee strong inspection once a year,causing a problem of extended service of medical devices,planted health risks to users. 
Medical institutions,strong sense of responsibility for the patient to recover "Although the quality of medical equipment,related to the life and health,but in the rights,whether institutions or the people themselves,are not strong enough sense of Responsibility."For example,you bought a home therapy device,found the problem to find manufacturers,manufacturers may apart from anything else and then replace it give you,you would not bother to chase a responsibility;If you buy a mask,Band-Aid kind of low- value products,if found good,that is most readily throw away,even the manufacturers are not look for.In the medical institutions,large hospitals simply do not survive inferior equipment,and small organizations to buy quality if there are problems,that is,directly to the manufacturer for repair or replacement.Events occur as long as there is no real threat to the life,inferior products will be able to muddle through,the manufacturer will be able to avoid liability. 
It is understood that after the implementation of the"Medical Devices Regulations"issued in 2000,10 years,with the development and changes in China's medical equipment industry,which is not suitable for development of the industry situation even more prominent.For example,it is responsible for the chase would not provide details on the terms of the lack of bad product traceability system. 
The newly revised"Supervision and Regulation of Medical Devices"provides medical equipment enterprises,and use of medical equipment purchased should pass inspection documents the supplier qualification and medical equipment,establish inspection record system.The second class,third class medical equipment wholesale business as well as Class III medical devices retail business ventures,sales records system should also be established.Medical equipment unit shall keep the original data acquired Class III medical devices,and to ensure that the information traceability. 
No matter what the problem is now in the presence of the medical device market,the new draft amendments are introduced to the industry on a"safety valve",the management of medical devices and drug control in the same position.Of course,the law,also need to be strictly enforced to ensure excellent products,anesthesia ventilator industry health. Production will be the focus of regulation violations 
With the launch of the special action,the medical device industry consolidation horn sounded.The official said that for a false registration application behavior,the second will focus on remediation,Class III medical devices registration untrue behavior for the first time,carried out in accordance with the provisions of the second,three types of medical equipment for the first time to submit an application for registration of producers of information (focus is on clinical trials report) and verification of the authenticity of tissue samples of the production process,the registration link in the report focus on verification. 
Production is also a violation of content regulation.Disposable infusion equipment,single-use catheters (package) does not meet the criteria for raw materials and did not seek sterilization,condoms without filing unauthorized commissioned production,hemodialysis concentrates not according to the standard factory inspection,etc.,will be the focus of regulation. 
In the circulation,illegal operation and will be glued to commence remediation hype behavior.For example,experiential approach to unauthorized sales of the second,three types of medical equipment,unlicensed plain lead eyewear colored decorative contact lenses,hearing aids,did not seek storage and transport in vitro diagnostic reagents and other acts.Again,back pain,myopia,diabetes and hypertension sticking classes,physical therapy medical devices for illegal propaganda;without the approval or approval of the content of tampering unauthorized release illegal advertising,exaggerating the effectiveness and scope of the product;use of medical research institutes or specialists,patient name and image to do to prove the efficacy of advertising and other unlawful acts,etc.. 
The article comes from:http://www.medicalequipment-msl.com/htm/medical-device-book/Who-will-bear-the-responsibility-for-security-of-medical-devices.html

Monday, May 26, 2014

Choose suitable transducer to improve the efficiency,accuracy and reliability of Sleep apnea machine.

Sleep apnea is called snoring,which is a disease troubling many people and affects their sleep badly.It is a challenge for medical device manufacturers to cure this disease.In this paper,based on the solution to this problem,we analyzed kinds of transducer solutions uesd in sleep-related breathing equipment and explained the differences among them,Ventilator equipment which provides valuable technical ideas for manufacturers. 
Sleep apnea syndrome(snoring),which worries millions of patients heavily,refers to breath stop during sleep which can appear repeatedly to a frequency of hundreds of times per night and to a time length of one minutes or more per time.Snoring may leads to memory deterioration and weight imbalance,even hypertension,cardiovascular and cerebrovascular diseases if leave it alone.Besides,the sleep insufficiency and fatigue caused by snoring may turn into the culprit behind inductrial injury accidents and motor vehicle traffic accidents 
Ventilator equipment - MSLVM01 
One commonly used method of treatment is using PAP.Patients wear a Special mask when sleeping,which press some air into their Nostrils to prevent Suffocation.There are 3 forms of PAP: 
*CPAP(continuous positive pressure ventilator)provides definite stressed air continuously.This positive pressure can prevent UAO caused by upper airway collapse,which enables patients to breathe freely in case of apnea 
*Auto-PAP(automated positive pressure ventilator),can measure the resistance when breathing and adjust the air supply pressure by the magnitude of the resistive force to make sure every breath unimpeded. 
*Bilevel PAP(bilevel positive pressure ventilator)provides two kinds of pressure:suction of positive pressure and exhalation of positive pressure. 
The Portable ventilator machine detect the respiratory cycle via a gas mass flow sensor,which comforts patients more.Thus,it's more frequently used than those without this function. 
The gas mass flow sensor used in the sleep apnea machine must be equipped with high resolution and accurate sensing ability,so that it can sense the weak air change and control the MAF given to patients more accurately.Such sensors should measure the MAF more precisely and at the same time,sense the existence of air flow. 
Another important consideration is power dissipation.Lower power dissipation makes it possible for the respirator to be powered by battery,which promises more flexibility to the patients 
Ultimately,the noise produced by motor of the apnea machine should be controlled when patients try to sleep,which is important.It conflicts with the purpose of the Anesthesia Equipments when the noise affects patients' sleep. 
It's difficult for the motor to work if the sensitivity of pressure drop (pressure drop equals to he resistance of sensor) is too high.Thus a gas mass flow sensor and relatively low pressure drop is needed,or else it will add noise and reduce the motor's working life. 
The article comes from:http://www.medicalequipment-msl.com/htm/medical-device-book/improve-the-efficiency-accuracy-and-reliability-of-Sleep-apnea-machine.html

Choose suitable transducer to improve the efficiency,accuracy and reliability of Sleep apnea machine.

Sleep apnea is called snoring,which is a disease troubling many people and affects their sleep badly.It is a challenge for medical device manufacturers to cure this disease.In this paper,based on the solution to this problem,we analyzed kinds of transducer solutions uesd in sleep-related breathing equipment and explained the differences among them,Ventilator equipment which provides valuable technical ideas for manufacturers. 
Sleep apnea syndrome(snoring),which worries millions of patients heavily,refers to breath stop during sleep which can appear repeatedly to a frequency of hundreds of times per night and to a time length of one minutes or more per time.Snoring may leads to memory deterioration and weight imbalance,even hypertension,cardiovascular and cerebrovascular diseases if leave it alone.Besides,the sleep insufficiency and fatigue caused by snoring may turn into the culprit behind inductrial injury accidents and motor vehicle traffic accidents 
Ventilator equipment - MSLVM01 
One commonly used method of treatment is using PAP.Patients wear a Special mask when sleeping,which press some air into their Nostrils to prevent Suffocation.There are 3 forms of PAP: 
*CPAP(continuous positive pressure ventilator)provides definite stressed air continuously.This positive pressure can prevent UAO caused by upper airway collapse,which enables patients to breathe freely in case of apnea 
*Auto-PAP(automated positive pressure ventilator),can measure the resistance when breathing and adjust the air supply pressure by the magnitude of the resistive force to make sure every breath unimpeded. 
*Bilevel PAP(bilevel positive pressure ventilator)provides two kinds of pressure:suction of positive pressure and exhalation of positive pressure. 
The Portable ventilator machine detect the respiratory cycle via a gas mass flow sensor,which comforts patients more.Thus,it's more frequently used than those without this function. 
The gas mass flow sensor used in the sleep apnea machine must be equipped with high resolution and accurate sensing ability,so that it can sense the weak air change and control the MAF given to patients more accurately.Such sensors should measure the MAF more precisely and at the same time,sense the existence of air flow. 
Another important consideration is power dissipation.Lower power dissipation makes it possible for the respirator to be powered by battery,which promises more flexibility to the patients 
Ultimately,the noise produced by motor of the apnea machine should be controlled when patients try to sleep,which is important.It conflicts with the purpose of the Anesthesia Equipments when the noise affects patients' sleep. 
It's difficult for the motor to work if the sensitivity of pressure drop (pressure drop equals to he resistance of sensor) is too high.Thus a gas mass flow sensor and relatively low pressure drop is needed,or else it will add noise and reduce the motor's working life. 
The article comes from:http://www.medicalequipment-msl.com/htm/medical-device-book/improve-the-efficiency-accuracy-and-reliability-of-Sleep-apnea-machine.html

Tuesday, May 20, 2014

Centrifuge widely used in medical healthcare sector.Domestic manufacturing sector getting transformation.

Over the past few years,domestic healthcare manufacturing sector getting transformation which objectives require greater ability to benchtop centrifuge.To make sure centrifuge characteristic,healthcare manufacturing need to fulfill requirement to <>.Those devices surface immediate contact with drug should clean,tidy,no death angle,easy to clean or sanitize,corrosion resistance,chemical change or adsorption will not take place with drug. 
Actually,centrifuge widely used in healthcare sector,especially in hematology separation,virus research,DNA research,medicine refinery.etc.Pharmaceutical Pharmaceutical centrifuge has several features like:flexible,high-automated,operation stable,strong handicraft property,good corrosion resistance,good operating environment,fully safety protection device reliable and attractive appearance etc.Medicine refinery other drugs used in the refining process was generally low-speed centrifuge(High speed centrifuge),rotation rate lower than 4000R,huge throughput,in order to meet drug production GMP specification and requirements,generally use flat stainless steel materials. 
Hematocrit centrifuge 
Pharmaceutical centrifuge has following advantage from function aspect:
1.flexible material,appropriate filter medium not only can separate millimeter fine particle but also can clean article through water pipe.
2.Artificial upper unloading type structure is simple,easy installation,low cost,easy to operate,can maintain the shape of the crystal products.
3.Machine adopt advanced resilient support structure,can reduce the vibrations caused by uneven load,smooth operate.
4.The whole high speed operating structure,concentrated in a closed shell,not only can achieve closed but also avoid contaminate materials.

All of Centrifuge corners,the corner welds are ground in the production process had a smooth rounded transition,as much as possible eliminate bump,health corner,effusion,plot materials and other corner.Experts advice:customers choose refrigerated centrifuge suitable materials should according to materials corrosion resistance feature,cleanliness when they choose centrifuge. 
The article comes from:http://www.medicalequipment-msl.com/htm/medical-device-book/Centrifuge-widely-used-in-medical-healthcare-sector.html