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Design of medical equipment |
Design of medical equipment
Concepts of implementing medical facilities
Medical device design patterns are analyzed and evaluated by the FDA.
To ensure the use of appropriate quality assurance models in the implementation of medical facilities and compliance with the requirements and requirements of the global quality system, the FDA has revised the requirements of the appropriate modern construction model by incorporating quality system rules. A key component of this review is the addition of acquisition nodes.
Because implant handling should be used in a variety of medical products. These laws reproduce the patterns of work that manufacturers are required to use during product development or to take over the product packaging process. These business models provide the flexibility needed by manufacturers to develop and expand impregnation suppliers, which are the FDA’s acceptance of the rules and most desirable for the impregnation and construction process.
Design of medical equipment
In addition to FDA regulations, the five basic ways to implement medical facilities are: being smaller, being able to wear implants, being wireless, being reliable, and being smart. These methods occasionally impose a range of barriers and confront the designer with implementation issues and difficulties regarding the implementation of medical facilities.
Being smaller
Wearable features for the patient should be small and well-designed so that they can be easily worn, tucked under clothing, or attached to a cloak, or identified as everyday accessories, such as a watch, a Disk Player. Or that belt. Therefore, later packaging should be reduced according to size and weight.
Design and manufacture of medical equipment
Design of medical equipment
At the same time, designers now want to add more functionality to medical products and facilities, which is directly inconsistent with the intention to implement smaller packages. Adding functions to the environment requires energy, energy, and heat. Electronic components, screen paper, batteries, sensor and sensor connectors, and power compete for enclosed space, power, and cooling. Determining components based on size, power consumption, packaging techniques, and heat management have all become part of the implementation considerations.
The need for micro-minimization extends beyond the scope of electronic possibilities to include small-scale visual and mechanical components. Essential technologies such as mechanical and electronic micro systems and even nanotechnology details for medical and biomedical applications are now being developed. Fortunately, all of these technologies are used in small electronic devices and products, such as telephones.
Design of medical equipment
Ability to wear, implant and implant
Medical devices that have the ability to be worn and placed in the body, belong to the batteries that are an important source of power. The overall strength criterion lowers the battery size, age and performance of the product. Wearable medical facilities can have rechargeable batteries. However, in medical facilities that are used at the request of implants and implants in the body, the age of the battery as a power source is essential and any placement requires surgical procedures. Charging can be an option, but it depends on the recipient / patient having access to the device as needed. This is an inevitable risk argument.
Design of medical equipment
Medical facilities that can be implanted and covered usually have direct contact with the human skin, which creates barriers to implantation. All medical facilities that have direct contact with the body must be biocompatible with the human body (surgical steel, gold and jewelry, surgical ceramics, glass, silicone, etc.). Biocompatible materials should be based around the body’s physiology, free from decay and decay. These materials must be non-toxic to body cells or be surrounded by non-toxic materials that act as a kind of isolation coating. Bio-compatible materials should have flexible surfaces to avoid irritating tissue and nerve damage, should not be sharp or heavy, and should have the flexibility needed to be used in flexible and natural body tissue. Human beings enjoy.
Products that have the capability and possibility of implants must be closed and free of seams and not allow the penetration of body fluids or contaminants. Also avoid leaking internal compounds, chemicals and liquids. The biocompatibility of the material is necessary to protect the sex, in other words, the standard that protects the patient.
Design of medical equipment
New methods in designing medical equipment
Being wireless
Whether the medical facilities used in hospitals or the medical facilities used in the doctor’s office or at home are moving towards wireless. A range of technologies used for this purpose include WMTS, BlueTooth, Wi-Fi, GPRS, GSM and IR. The cause is obvious: permission for the patient to have freedom of movement in the hospital or to leave the house free of collisions with cables.
Some new products can be remotely accessed and monitored while giving the doctor direct and indirect access to patient data in addition to physical presence. These data features