Clean Disinfect Track & trace Store


1965


Since the 1960’s, everything changed, but gloves didn’t. Does this make sense?


Why do healthcare professionals use gloves with a high percentage of defects? If conventional gloves are not produced in a controlled environment, can they be considered


safe and clean? Does it make sense to believe that a medical device packed in a cardboard box (porous


2023


material) that travels in containers on ships for about 2 months before reaching its destination is safe to use on healthcare professionals and patients?


How can we trust packaging that is not airtight before being opened and cannot be cleaned


on the outside when touching potentially contaminated surfaces? Why can't professionals remove gloves from the packaging by the cuff, as recommended by


the WHO since 2009?1


So... what if... we could improve protection? The R.ADVANCE Single Use Examination Nitrile Gloves were designed to change the protection standards


Lowest AQL2 in the World: 0.25


100% inspected gloves instead of a single random batch like standards3 86% less risk of finding a glove with punctures or micro-punctures* Single-Glove Extraction by the Cuff, as per WHO guidelines4 Air and watertight packaging, decontaminated at the production line Packaging that can be desinfected whenever necessary


The Safest Glove


(1)(4). World Health Organization. Glove Information Leaflet. 2009. (2). Acceptable Quality Limit | The lower the AQL, the safer the glove is (EN 455-1:2020).


(3). Following norm ISO 2859, for an example batch of 4 million gloves, 500 random gloves are analyzed. * When compared to Standard Gloves (AQL 1.5).


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