Bots 'N Brains

"To be prepared is half the victory" - Miguel De Cervantes

Oxygen Concentrators are one of the most critical items in this pandemic and we are proud to bring it to you with our post sales service guarantee.

After many inputs from Doctors in our society about
post sales service issues and fraudulent companies selling substandard product at higher prices it is the need of the hour to be assured of the product and after sales service when you make a purchase.

We are a company founded by IIT and IIM Alumni trusted and partnered with Indian Academy of Orthopaedic Surgeons, you can read about us here www.iaos.online and www.botsnbrains.com

If you would like to know anything about oxygen concentrators even outside our product, you can whatsapp us by clicking on this link.
We are just a message away.
https://wa.me/917755945825/?text=I+want+to+buy+JLO590si+5L+Oxygen+Concentrator

To book Model 1 online please follow the link
https://rzp.io/l/WTdKHON

To book Model 2 online please follow the link
https://rzp.io/l/JHsV5CLL

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The Coronavirus lockdown circumstance ahas made India focus more on medical device fabrication in India. Manufacturers have long requested the government to reduce GST on devices to 5 % from the current 18 %.
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CDSCO is fundamentally answerable for guideline of medical devices. Manufacturers GMP and conduct reasonable tests to demonstrate the device quality.

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Medical devices in India has been divided into classes. The classes are named as Class A that includes devices of low danger, Class B as low moderate danger, Class C as moderate high danger, and Class D as high danger.

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Medical device authorities need to ensure that clinical gadgets are as accurate as could reasonably be expected. But the idea of accomplishing and keeping up administrative consistence wory manufacturers.

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FDA has to ensure that medical devices are as protected as could reasonably be expected. Manufacturers need to pass all these regulation. And the idea of accomplishing and keeping up administrative consistence may wory some firms.

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The Indian government has set out the timeline for moving to another administrative framework. Authorities plan to establish a law for the oversight of all devices. The change may increase the sales of medical devices in India

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India Medical Device Regulations and the Indian clinical administrative framework have gotten more confounded as of late. There are around 30 equipment "families" that layout which explicit medical equipment should be enlisted.
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Disposable Syringes are being used by doctors to inject medicines through intravenous or intramuscular ways for the treatment of diseases & also by research & development personnel.
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In vitro diagnostic products are those reagents, instruments, and systems intended for use in diagnosis of disease or other conditions, including a determination of the state of health
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The European Medical Device Regulation (MDR) is a new set of regulations that governs the production and distribution of medical devices in Europe, and compliance with the regulation is mandatory for medical device companies.
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Some products are designed specifically for children, while others are borrowed from adult applications or produced for more general use. Designing pediatric medical devices can be challenging
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