Polyco Finite P Indigo AF Nitrile Powder Free Exam Gloves

Finite® 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.

Product Colour Purple

Size Range XS - XL

Fingertip Thickness 0.08 mm

Palm Thickness 0.06 mm

Typical Weight 4.20 g

Shelf Life 3 Years

• Chemical Resistant: Achieves type B chemical resistance according to EN ISO 374-1, for protection against at least 3 different chemicals
• EN ISO 374-5 Protection: Conforms with the requirements of EN ISO 374-5, for protection against bacteria, fungi and virus
• Fit: Unique shape delivers a glove with improved fit
• Food Safe: Suitable for food contact all food types. Please refer to our online Food Compatibility Chart for full details
• Sensitivity: Accelerator free, Removing the risk of contact dermatitis caused by accelerator chemicals Latex free, reducing the risk of hypersensitivity and allergic reactions to natural rubber proteins
• Comfort: Nitrile technology provides an exceptionally soft and pliable material
• Powder Content: Powder Free, reducing the risk of dust contamination
• Suitability: Suitable for use with cytotoxic/chemotherapy drugs
• Silicone Free: Silicone residues from gloves can interfere with painting, coating, or adhesive bonding processes, potentially causing defects. These silicone-free gloves help minimise that risk, ensuring clean application surfaces.

Disposable Gloves Standards

• AQL 1.5
• Compliant with European Standards EN455: Medical Gloves for Single Use parts 1,2,3&4
• EU Certified
• Manufactured in accordance with Personal Protective Equipment (PPE) by the European PPE Regulation (EU) 2016/425
• Tested in compliance with Commission Regulation (EU) No 10/2011 for Food contact
• Tested to European standards EN420, EN ISO 374-1, EN ISO 374-4 & EN ISO 374-5
• 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)