Box 100 Finite P Indigo Accelerator Free Nitrile Disposable Gloves MFNP100

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Product details

Management number	204843136	Release Date	2025/10/28	List Price	$46.50	Model Number	204843136
Category	Work Gloves Glove Brands

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

Packing Contents - All: 100 gloves per dispenser, 10 dispensers per case, 60 cases per pallet

Size Range: XS - XL

Fingertip Thickness: 0.08 mm

Palm Thickness: 0.06 mm

Typical Weight: 4.2 g

Product Highlights

Achieves type C chemical resistance according to EN ISO 374-1, for chemical protection against at least 1 chemical

Conforms with the requirements of EN ISO 374-5, for protection against bacteria, fungi and virus

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

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)