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Advice from the BP Measurement Experts

Complete Product Registration & You Might Just Get A Raise!

Picture of a Finger pressing a Register Button

We all see the card that comes with our new gadget, encouraging us to register our product online, and give it a furtive glance. But many times, that gets quickly forgotten or put into the ever-mounting pile of “to dos” that you will get to in your “free time.” Rather than list all of the reasons that product registration is important, here is what I intended to be a clever way of reviewing the benefits of completing this process…

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New 3rd Edition Standards for NIBP (Part 2)

OEM NIBP from SunTechIn my last blog post I provided 4 out of 8 new 3rd edition regulatory requirements that impact automated non-invasive blood pressure. These included out of range values, nominal blood pressure ranges, service modes and shock/vibration changes. Here are the final four regulatory requirements that must be addressed if you are designing a product with your own non-invasive blood pressure (NIBP) or with NIBP supplied by an OEM provider.

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New 3rd Edition Standards for NIBP (Part 1)

Medical Design RegulationIf you're a medical device developer or active in the design process, you've probably been involved with creating a list of "must have" and "nice to have" features and requirements for a new or updated medical device. Some come from market feedback, industry trends, competitor analysis, R&D and others come from medical equipment Regulatory standards. When it comes to safety and meeting regulatory standards, this is always in the mandatory column. With several deadlines looming on the horizon, meeting the latest 3rd edition standards as well as being RoHS compliant are on almost everyone's must have list when starting a new project. So whether you are developing your own NIBP or purchasing OEM NIBP modules, you now have new requirements that need to be a part of your design not only in hardware and software but also in the product's technical documentation.

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Regulatory Changes: Are you prepared?

Street sign at the corner of Healthcare End and Reform WayThe regulatory world is changing. Countries are examining and changing the rules and regulations that govern the way businesses interact and make an impact. In the US, with his editorial article in the Wall Street Journal and his State of the Union Address, President Obama makes a clear message about government regulatory systems. He wants balance between commerce & safety, progress & common sense. Obama calls for regulations to be reviewed so that the US “(protects its) safety, health and environment while promoting economic growth.” While the call to update regulations is clear, the balance that is called for lies in a well-known, well-trodden, broad, gray area. It’s this same area that all countries are trying to define, regulate, and enforce for the good of their citizens.

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CMEF 2010: China and Growing Awareness of Hypertension

SunTech Medical at CMEF 2010Earlier this year we wrote a blog post about the similarities of current healthcare challenges in both China and the US. Of particular note was the fact that Hypertension is the leading cause of premature deaths in China. We recently had an opportunity to meet and speak with many folks involved with the delivery of healthcare in this rapidly evolving market at the China Medical Equipment Fair (CMEF) held in Shenzhen April 18 - 21, 2010.

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2009 Medica Fair Attracts Medical Device Industry

MEDICA 2009

Highlighting the Importance of Clinical Grade Blood Pressure Technology

On the week prior to the Thanksgiving Holiday in the US, several personnel from SunTech Medical attended the 2009 MEDICA International Trade Fair in Düsseldorf, Germany. Over the four days of this event, (November 18 - 21), the world's largest medical trade fair hosted nearly 138,000 trade visitors from over 100 countries and 4,324 medical industry exhibitors from 60 different nations.

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