Snuza has been developing baby movement monitors, using leading edge bio-sensory technology, since 2007. Our monitors are aimed at monitoring a baby’s breathing movement and alerting parents of any incidents where the breathing movement has stopped. Snuza is a young, innovative and dynamic company, and the first baby tech company to have successfully introduced a portable baby movement monitor and also the world’s first portable baby breathing monitor. The Snuza team consists of motivated and dedicated individuals driving the development and distribution of baby monitors that speak for babies who are unable to at their most vulnerable moment - when they're alone in their crib and unable to breathe.

Where did it all begin?

Founder, Greg Gallagher shares the story behind Snuza

In 2003, I was introduced to the concept of baby breathing motion monitors. At the time, there was no such thing as a portable monitor. All products on the market were bulky and required wall power with wires, mats and all sorts of things that appeared dangerous (I'd heard of a case of strangulation in one instance). With a background in electronics engineering and having set up my own business a few years prior, I set out to develop a portable breathing monitor for babies that exceeds the performance of anything on the market. Although SIDS (Sudden Infant Death Syndrome) and SUID (Sudden Unexpected Infant Death) are not scientifically proven to be a result of a cessation of breathing, I could not help think how devastating it must be for a parent to lose a child this way, without giving them an opportunity to at least try to resuscitate their little one, if such an event had to occur. Statistically speaking, providing this opportunity seemed far important than anything else since according to CDC data (USA stats), a baby is 20 times more likely to die from SIDS/SUID than in a car accident. Yet seat belts and approved car seats are a legal requirement in most of the developed world.

After nearly 5 years of R&D, including countless hours at the NICU unit testing alongside "gold standard" hospital equipment, we finally had a product that was ready for the market. The design, certification, branding, patents and company structure were complete, now it was time to let the world know about us. We initially approached various retailers in South Africa, none of whom showed interest. Perhaps it was too early for the South African market! So in the interests of getting a device to market sooner rather than later, we shifted our attention to the rest of the world. We packaged the Snuza Hero (Called the “Halo” back then), and traveled across the globe to various baby trade shows such as Kind Und Jugend in Germany, the ABC show in Las Vegas USA, the CBME show in China, to name a few, in the hope of building a network of contacts interested in investing in our idea and product, and hopefully to represent us in their respective countries.

It was a very slow start but eventually Snuza began to gain traction. It was a bumpy first few years, streamlining production and our internal systems to handle the load of increased demand taking its toll. There were certainly growing pains but things gradually improved. As sales in the rest of the world were increasing, which helped establish the brand, we were getting our company’s management system up to "Medical Device" ISO 13485 standards. Snuza HeroMD is now a certified Class IIb Medical Device (MDD 93/42/EEC), clinically proven to be able to detect when a baby stops breathing. This was a huge achievement and a world first. Our "Post Market Surveillance" enabled us to conservatively estimate that our devices have accumulated over 1,000,000,000 (1 billion) hours of use by well over 350,000 users.

Having a certified medical device on the market, with incredibly strict requirements not only in product design (safety, proven efficacy, etc), manufacturing and testing, but also in company operating procedures, allowed us to collect data we would never otherwise have been able to collect. The average worldwide SIDS rate is about 1 death per 2000 births. In Snuza's case there have been 350,000 devices used with (very sadly) one reported death (the device performed as expected but the baby could not be resuscitated). Without Snuza, this number would be closer to 175 deaths. It's horrific to talk about death in cold statistical terms, but this is the reality. What's perplexing and tragic is that most paediatric associations around the world discourage the use of such monitors because "there is no clinical evidence that these monitors reduce SIDS". Are these organisations saying that there is no chance of resuscitating a baby in the event that they stop breathing? What clinical evidence do they have to support this stance? In the meantime 10 babies is the US alone die each day due to SIDS/SUID.

Our team of talented and dedicated individuals have ensured our steady growth to the point where we are one of the largest baby movement/breathing monitor brands in the world, and our commitment to continuous improvement and furthering research will hopefully one day help to reduce the number of babies who are lost to SIDS/SUID. In fact, 

Every so often a testimonial comes across my desk of a life changing event, where our little Hero acted as the voice for a baby that could not. That is what drives me.