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PneumaPure® filter technology approved by the Saudi Food & Drug Authority

SleepAngel Medical Barrier Bedding is now officially approved and registered with the Saudi Food & Drug Authority in Saudi Arabia.

SleepAngel Medical Barrier Bedding by Gabriel Scientific is now officially approved and registered with the Saudi Food & Drug Authority in Saudi Arabia.

PneumaPure® filter technology for soft surfaces is also certified as Class I Medical Device in EU and Registered Class I Medical Device within the FDA.

The Saudi Food and Drug Authority (SFDA) is an independent body corporate that directly reports to The President of Council of Ministers. The main objectives of the SFDA is to ensure safety of food, drug for human and animal, safety of biological and chemical substance as well as electronic devices that related to human health. SleepAngel Medical bedding is one of the only soft surfaces that belong under medical device category. Previously already Registered as Class I Medical Device within the EU and Registered Class I Medical device within the FDA.

Read more about the SFDA on their homepage – The Saudi Food and Drug Authority (SFDA) 

“Soft surface contamination, sustainability and infection prevention are the subject areas we we work on every day. Receiving approval from SFDA, FDA and EU and being recognised as a medical device is a big support for our daily challenges,” says Sven Jürisoo, CEO and founder of Gabriel Scientific, producer of SleepAngel® Medical Barrier Bedding – the first barrier bedding range to combine absolute barrier protection with airflow.

 

Find the distributor database for SleepAngel Medical on our webpage or contact us directly info@SleepAngel-Medical.com

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