Nitrex Accelerator Free Blue Nitrile Glove GN06 ideal solution for those sensitive to thiurams, carbamates or thiazoles.

Description

NITREX Accelerator-Free examination gloves are manufactured using a unique technology that negates the requirement for sulphur and chemical accelerators during the manufacture process. As such the glove provides an ideal solution for those sensitive to thiurams, carbamates or thiazoles.
The technology utilised to produce NITREX Accelerator Free examination gloves reduces the risk of Type IV Hypersensitivities caused by residual chemical accelerators.
Product Colour: Blue
Packing Contents – All: 200 gloves per dispenser, 10 dispensers per case, 36 cases per pallet
Size Range: XS-XL
Fingertip Thickness: 0.07 mm
Palm Thickness: 0.06 mm
Typical Weight: 3.7 g
Product Highlights

Accelerator free, Removing the risk of contact dermatitis caused by accelerator chemicals
Achieves type B chemical resistance according to EN ISO 374-1, for protection against at least 3 different chemicals
Conforms with the requirements of EN ISO 374-5, for protection against bacteria, fungi and virus
Grip:

Textured finish to the fingers to enhance grip and handling
Food Safe:

Suitable for food contact; all food types. Please refer to our online Food Compatibility Chart for full details
Sensitivity:

Latex free, reducing the risk of hypersensitivity and allergic reactions to natural rubber proteins
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 EN ISO 21420, 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)