Finite P Indigo AF Nitrile Accelerator Free Powder Free Exam Glove
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SKU
BRDI_SA_MFNP100

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Brosch Direct, a trading division of Polyco Healthline Ltd

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Finte P Indigo AF Nitrile Accelerator Free Powder Free Exam Glove are medium weight and medical grade designed for optimal protection and comfort. The accelerator-free properties of this glove eliminate the risk of contact dermatitis, while the latex-free design reduces the risk of allergic reactions.
Unit | Box of 100 |
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Key Features | <div class="product attribute extra"><div class="product attribute extra"><strong class="type">Food Safe : </strong><ul class="attr-data"><li>Suitable for food contact; all food types. Please refer to our online Food Compatibility Chart for full details</li></ul></div><div class="product attribute extra"><strong class="type">Sensitivity : </strong><ul class="attr-data"><li>Accelerator free, Removing the risk of contact dermatitis caused by accelerator chemicals</li><li>Latex free, reducing the risk of hypersensitivity and allergic reactions to natural rubber proteins</li></ul></div><div class="product attribute extra"><strong class="type">Comfort : </strong><ul class="attr-data"><li>Nitrile technology provides an exceptionally soft and pliable material</li></ul></div><div class="product attribute extra"><strong class="type">Powder Content : </strong><ul class="attr-data"><li>Powder Free, reducing the risk of dust contamination</li></ul></div><div class="product attribute extra"><strong class="type">Suitability : </strong><ul class="attr-data"><li>Suitable for use with cytotoxic/chemotherapy drugs</li></ul></div></div> <div class="product attribute extra"><ul class="value"><li>AQL 1.5</li><li>Compliant with European Standards EN455: Medical Gloves for Single Use parts 1,2,3&4</li><li>EU Certified</li><li>Manufactured in accordance with Personal Protective Equipment (PPE) by the European PPE Regulation (EU) 2016/425</li><li>Tested in compliance with Commission Regulation (EU) No 10/2011 for Food contact</li><li>Tested to European standards EN420, EN ISO 374-1, EN ISO 374-4 & EN ISO 374-5</li><li>This product is classified as a Class I Medical Device in compliance with the requirements of Medical Device Regulation (EU) 2017/745 & UK MDR 2002 (SI2002 No.618 as amended) (UKCA)</li></ul></div> |
Features | 1 |
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