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PRODUCTS & SERVICES


UNIGLOVES AND KLURALABS LAUNCH ANTIMICROBIAL


NITRILE GLOVE Unigloves, a specialist in hand protection, and KluraLabs, innovators in antimicrobial solutions, have partnered to launch the CrossGuard antimicrobial nitrile glove, the first of its kind to eliminate 99.99% of selected bacteria in just 60 seconds. This breakthrough is backed by third-party testing and is free from active ingredients.


Revolutionary antimicrobial protection


The CrossGuard glove leverages KluraLabs’ advanced antimicrobial technology, optimising the surface chemistry of standard nitrile gloves by adjusting material levels to create a safe and effective antimicrobial product. These gloves provide unmatched protection against bacteria within one minute, making them ideal for use in healthcare, laboratory, and food processing environments, where infection control and cross-contamination prevention are critical.


Chris Wahlers, Managing Director of Unigloves UK, said: "Hands are often a primary source of infection.


By delivering 99.99% defence against bacteria in just 60 seconds, CrossGuard represents a significant advancement in infection control. This innovation sets a new standard for protection in hospital, care, and food handling environments."


Key benefits of CrossGuard Antimicrobial Gloves:


● Enhanced patient safety: Helps prevent the spread of hospital- acquired infections (HAIs), reducing risks for both patients and healthcare providers.


● Cross-contamination control: Reduces contamination risks in food manufacturing, processing and handling sectors.


● Sustainability: The antimicrobial technology is made from non- toxic, non-leaching materials that are environmentally friendly. These gloves require no special disposal measures.


ZOLL AED PLUS RECEIVES APPROVAL FOR AEDS UNDER THE


EU MDR CERTIFICATION ZOLL, an Asahi Kasei company that manufactures medical devices and related software solutions, has announced that the ZOLL AED Plus defibrillator is approved under the European Union (EU) Medical Device Regulation 2017/745, commonly referred to as EU MDR. The ZOLL AED 3 received MDR approval in January 2024.


EU MDR is the European Union Medical Device Regulation 2017/745 that was adopted in 2017 by the European Parliament and the Council of the European Union. The intent of the EU MDR is to ensure a high standard of safety and quality for medical devices that are produced in, or supplied to, member countries of the European Union.


ZOLL now has CE marking for the ZOLL AED Plus defibrillator under the EU MDR.


Elijah White, President of ZOLL’s Acute Care Technology division, said: “ZOLL is happy to have received our second MDR certification for our AED Plus. With this new


x.com/TomorrowsHS


Blake Gudgel, CEO of KluraLabs, added: "Healthcare-associated infections are a serious challenge. Using real science, we’ve developed CrossGuard to reduce the transmission of bacteria and viruses, making a real impact in infection control without compromising safety or fit.”


The CrossGuard gloves also offer comfort, flexibility, and durability, including touchscreen compatibility and a wide range of sizes to suit all users.


Chris Wahlers concluded: "CrossGuard reflects our commitment to sustainability, innovation, and customer-focused solutions. We’re proud to offer a product that not only delivers top- tier performance but also minimises environmental impact."


https://uk.unigloves.com/products/crossguard-nitrile https://uk.unigloves.com


certification, ZOLL customers will know that this device has passed the most stringent level of European medical regulation for a medical device.”


ZOLL continues to work diligently toward achieving EU MDR approval for the Powerheart G5 and certification for ZOLL’s full portfolio of products.


www.zoll.com www.asahi-kasei.com


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