A Medical Equipment is device intend to be used for medical purposes. Thus what differentiates a medical device from an everyday device is its intended use.
We repair unworkable parts to enhance the life of the machines to get accurate results at the best cost.
So, Medical devices benefit patients by helping health care providers diagnose and treat patients and helping patients overcome sickness or disease, improving their quality of life.
However, Significant potential for hazards are inherent when using a device for medical purposes and thus medical devices must be proved safe and effective with reasonable assurance before regulating governments allow marketing of the device in their country.
The regulatory authorities recognize different classes of medical devices based on their potential for harm if misused, design complexity, and their use characteristics.
So, Each country or region defines these categories in different ways. The authorities also recognize that some devices are provided in combination with drugs, and regulation of these combination products considers this factor.
Decrease reimbursement costs
- Improve the quality of care
- Improve patient satisfaction
- Increase efficiency
- Cost control
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