Thermometer medical device

Freyr provides end to end regulatory support for medical device & IVD manufacturers in product registration, notification, classification across the globe. https://medicaldevices.freyrsolutions.com/

Operon Strategist is a medical device consulting companies which provides regulatory guidance to various manufacturers in the healthcare industry to ensure the strategic development of these manufacturers.

We “Cliniva Healthcare” are a leading Manufacturer and Exporter of a wide range of Hospital Equipment Manufacturers & Professional Hospital Supply,Medical Instruments, Urology Instruments, Laparoscopy Instruments And Hospital Medical instruments, Health Care instruments or healthcare facility required products Many More in India, US & UK.The warehousing facility has a large number of shelves, which are sequentially marked, so that we can place the packaged products in accordance with their categories. Visit For More: https://clinivahealthcare.com/ Address: G/57, Sahjanand business Park,Near Keshwam estate, Near S.P.Ring Road, Kathwada GIDC, Nikol, Ahmedabad-382430.

Our patient monitor is medical devices that are used to monitor the health of a patient. Patient Monitoring is one of the awe-inspiring technologies, the brainchild of advanced science that serves as a tool in taking care of millions of lives. Our patient monitor is medical devices that are used to monitor the health of a patient. Patient Monitoring is one of the awe-inspiring technologies, the brainchild of advanced science that serves as a tool in taking care of millions of lives. Package Includes: 12.1” TFT Color LCD Display. With Standard interface, Oxygen graph, tent graph, big character interface and view bed, convenient to observe. Finish all operations by keys and knobs. Maximum 8-channel waveform synchronous display. Display 7-lead ECG waveform on one screen, cascade ECG waveform display. Standard Parameter: SpO2 NIBP ECG RESPIRATION TEMPERATURE Contact Us: Medicosys Pvt Ltd, Behind BSNL Tower,Sindagi Road,Indi, Dist: Bijapur, Vijayapura, Karnataka - 586209 Email: show contact info Phone: 7020208763 Website: https://www.medicosys.in/

Diploma / Degree - Mechanical with minimum 5 - 10 years of experience in related field. Knowledge of electrical circuits, PLC operations, HMI, Automation is preferred. Planning and undertaking scheduled maintenance. Responding to breakdowns. Diagnosing faults and repairing equipment. Supervising engineering and technical staff. Managing stocks of supplies and equipment. Ensuring smooth running of Prime Placement and Manpower Services We are Leading Placement Consultant in Ahmedabad. We require Production & Maintenance Engineer for our Client a Leading Manufacturing Company Located at Changodar - Ahmedabad - Gujarat.machinery. Quick learner. Email@vinod@primeplacement.in / primeplacementadi@gmail.com T.no:7777981967

ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. This certification is not a requirement of the ISO standard like other ISO management system standards have. Without going through the certification process an Organization can reap the benefits by implementing the standard. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

ISO 13485 Standard clauses and requirement are applicable to all types of organizations irrespective of size or nature and applicable to all like Hospital, Health Care, Trading, Manufacturing, Service Companies, Software, Construction, and Medical Devices in India. URS offers ISO 13485 Certification in all cities, in Mumbai India. ISO 13485 certification for Medical Device has been developed so that the medical industry does not compromise with public safety and health. This certification ensures that the companies follow all the measures to produce quality products as per the global standards. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

ISO 13485 - Quality Management System in Solan clauses and requirement are applicable to all types of organizations irrespective of size or nature and applicable to all like Hospital, Health Care, Trading, Manufacturing, Service Companies, Software, Construction, and Medical Devices in India. ISO 13485 Certification in Noida works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. This certification is not a requirement of the ISO standard like other ISO management system standards have. Without going through the certification process an Organization can reap the benefits by implementing the standard. Stay tuned with us to know more Insight on this standard and also please visit our website www.ursindia.com to know more about other standards. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Mobile: +91-9650807813

Are you at Risk of Heart Attack- Sibia Medical Centre Heart disease is the leading cause of death in India. The term “heart disease” refers to several types of heart conditions. The most common type is coronary artery disease, which can cause heart attack. Anyone, can develop coronary artery disease. It occurs when a substance called plaque builds up in the arteries. When this happens arteries can narrow over time and reducing blood flow to the heart. Increasing age, smoking, eating unhealthy foods, not getting enough exercise, high cholesterol, high blood pressure or diabetes can increase risk for heart disease. Anyone above 40 years or having these risk factors should undergo annual cardiac check. Besides Electrocardiogram, Treadmill test, Coronary CT angiography, etc. now a new device called Cardiovascular Cartography (CCG) is available to evaluate cardiac status. Cardiologists may become increasingly depend to diagnose heart ailments non-invasively with CCG’s 3D map heart flow map. CCG is a technique for early detection of coronary artery disease (CAD) to evaluate the functional status of the heart and plan further treatment. For CCG test the patient is "wired" to CCG device using electrodes and a highly sensitive transducer while the patient is lying down. If required the test can be repeated after a drug to see effect of mild stress on the heart. CCG can also be used to evaluate a drug’s effect on the heart’s function. Within minutes of giving a tablet of sorbitrate the redistribution of blood flow to the heart muscle is shown by the CCG. A high-speed computer makes all calculation and result is available within 15 minutes. Such data was earlier not possible through non-invasive methods. The records obtained include details such as the amount of blood pumped for every beat of the heart, pressure, volume and time relationship, relative oxygen demand, and much more. The CCG heart blood flow map has a positive predictive accuracy of over 90 per cent and a negative accuracy of over 80 per cent in detecting heart disease. Angiography measures the quantity of blockages in the heart’s blood vessels but not the amount of blood reaching the heart muscle. While angiography tells us how much water is flowing in the river, CCG tell us the quantity of blood reaching the fields. What is more important? For the farmer the quantity of water actually reaching his crops is all that matters. He is not concerned with the how much water is there in the river. Blockages in the arteries are not the only factor deciding how much blood reaches the heart muscles. Angiography does not tell us how well the body has compensated itself for the decrease in blood flow caused by the blockages. This compensation attributed to collaterals, pressure changes, etc. is not well assessable with angiography. This is why we often see patients with 99 percent blocks moving around without chest pain or heart attack. It is gradually being realized that blood flow to the heart muscle is all that matters. It is decreased flow to the heart muscle that causes angina chest pain or heart attack. CCG’s painless mapping of the heart blood flow is an important tool to detect coronary heart disease early, to evaluate extent of disease or to know the effectiveness of a treatment. It is often used to evaluate, plan and study progress of non-invasive, non-surgical treatments such as Artery Clearance, Chelation Therapy, Ozone Therapy, External Counter Pulsation, Extracorporeal Shockwave Myocardial Revascularization. (SibiaMedicalCentre.com)

We provide consultation for Medical and In-vitro Medical Device CE, US FDA, NIOSH, ISO, and Indian MDR certification along with services like Appointment of Authorized Representative, External testing services, EUDAMED registration, UDI Labelling, Registration on Sugam portal, Country registrations, Internal Audits, Management Review Meetings, Training, GAP analysis & audits, Mock audits, Conformity assessment, Document review, and Audit NC closures. For clients who face limited challenges in specific documentation, we also provide a customized service of preparing individual documents or parts of it. Our training & consulting support helps medical device customers to design & manufacture their products in compliance with regulatory requirements and bring them to the market more quickly, effectively & efficiently.

Mechanical Design Engineer (SolidWorks) FRESHER AND EXP JD: Experience: Fresh / Experience, 0 to 2 Years Education: DME / B.E/ B.Tech in Mechanical Engineering Job Location: Chennai Job Description: The primary responsibility of the selected candidates will involve drafting and designing various products using SolidWorks specifically tailored for medical device manufacturing. Roles and Responsibilities: Engaging in all phases of new development, prototyping, test method design, design evaluation, design reviews, design specifications, design verification and validation, design protocols, and reports, and transfer to production activities in a timely effective manner. Product testing and evaluation, completion of test reports to support design selection. Organize projects and maintain Design History Files (DHF) Complete design drawings in Solid Works or a similar drafting tool and create prototypes to progress the development through its design stages Development of component specifications, inspection methods, bills of materials, and manufacturing processes. Introduction of new equipment, materials, and technologies. Manage and drive project tasks to ensure the timely completion of goals. Product performance evaluations. Contribute to innovation and creativity within the team through the filing of disclosures and patents. Hold regular goal meetings and document minutes and actions. Compliance with Quality, Regulatory, and company policies and systems. Qualifications: Experience in SolidWorks Solid Modelling, Surface Modelling, Assembly, Flow analysis b'&' Simulation DME / BE / B.Tech. Degree in Mechanical Engineering or Biomedical Engineering Knowledge of DMR / DHF (Design Plan, Design input/output, Validation b'&' Verification, and Design Transfer) would be an added advantage. Understanding of quality and regulatory requirements for medical devices classification A proven record of interpersonal skills to handle clients should be Result oriented and self-driven Industry Type: Medical Device Manufacturing Employment Type: Full-Time, Permanent Experience: Fresh/Experience, 0-2 years Edu: Dip / BE / Btech Location: chennai Regards, Nedhra -HR 89251 and 14937

BISI World was founded in April, 2019 with focus on 'Medical Equipment supplier in India' to 'bridge the information gap'on existing, innovative and costeffective devices. "Buy N95 Face Mask Online" BISI World is an “Medical Equipment supplier in India”. Our Business associates comprise of Hospitals, Doctors, MNCs, manufacturers, bulk suppliers/wholesalers/importers, Authorised dealers and sub dealers. We believe that our platform can create a 'conducive ecosystem for medical device sector' by opening up new avenues for trade of the medical devices. "Buy N95 Face Mask Online"

ISO 13485 QMS is specifically for medical devices and to provide much advantage for organization. This standard provide evidence to represent customers, organization follows global quality standard for manufacturing and designing of medical devices. ISO 13485 Certification works on continuous improvement in the compliance, quality management system laid down the foundation for medical device manufacturers and service providers. Stakeholders' confidence will build strength in manufacturers and service providers. This standard acts as a building block for quality management. URS offers UKAS and NABCB accredited ISO Certification services in all over India. If you are looking and interested to any ISO 13485 Certification, then Contact us for more information or visit URS website: URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Tel: 91-120-4516264 - 65 Mobile: +91-9650807813

The ISO 13485 is a certification measure that is like ISO 9001 but basically acts as a standard to measure best management practices in the health sector. ISO 13485 is an international standard intended to reassure organizations purchasing and utilizing medical devices that the developers and suppliers of these devices have instituted and implemented a QMS that meets certain minimum requirements, Suppliers and developers express their conformity and assurance to this level of medical device quality by becoming ISO 13485 certified. If a company or entity participates in or provides design and development, production, storage, distribution, installation, servicing or other technical support, their related operations most likely fall under the QMS standard. For more information and updates in the ISO 13485, keep an eye on the URS website. URS CERTIFICATION F-3, Sector 06 Noida- 201301, India Tel: 91-120-4516264 - 65 Mobile: +91-9650807813

Description: wanted for Regulatory Affairs Engineer Company: EDM SOFTWARE SOLUTION Location: Coimbatore, Tamil Nadu, India Description: EDM SOFTTECH SOLUTION PVT LTD COMPANY COIMBATORE 9791684242 Job Description: Company: Medical Equipment Manufacturing Industry Qualification: BE/Dip Mech Designation: Regulatory Affairs Engineer Exp: 4-5yrs Salary: 25-30k Location: Sulur, Coimbatore Skills: QMS Module, ISO documents and Medical Device field added advantage Skills: - Basic Skill - Communication Skill - Field Skill Fresher & experienced candidate both can apply Processing Time: 85 - 95 working days If you are interested kindly send your updated CV or contact us for more details Thanks and regards EDM SOFTTECH SOLUTIONS PVT LTD COMPANY COIMBATORE HR NO: 9791684242 / 9994241641 Email ID: edmsofttech@gmail.com