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GN06 Nitrex, Nitrile Gloves, Blue, Accelerator Free, S-XL Group Picture

GN06 Nitrex, Nitrile Gloves, Blue, Accelerator Free, S-XL

Excl. VAT Incl. VAT

£9.26 to £81.35

Code: Please choose option from drop down above
  Pack Size List Price Qty  
photo_camera S x 100 Pack
GN06-S-100
£9.26
photo_camera S x 1000 Pack
GN06-S-1000
£81.35
photo_camera M x 100 Pack
GN06-M-100
£9.26
photo_camera M x 1000 Pack
GN06-M-1000
£81.35
photo_camera L x 100 Pack
GN06-L-100
£9.26
photo_camera L x 1000 Pack
GN06-L-1000
£81.35
photo_camera XL x 100 Pack
GN06-XL-100
£9.26
photo_camera XL x 1000 Pack
GN06-XL-1000
£81.35

Nitrex Accelerator Free Blue Nitrile Glove
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
Size Range: S-XL

  • Household cleaning
  • Light DIY tasks
  • Laboratory work
  • Engineering
  • Automotive
  • Medical
Accelerator Free:
  • Accelerator free removing the risk of contact dermatitis caused by these chemicals
Grip:
  • Textured fingertips provide an improved grip and optimise surface performance in both wet and dry conditions
Latex Free:
  • Latex Free reducing the risk of hypersensitivity and allergic reactions
Powder Free:
  • Reduced 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 to European standards EN ISO 21420, EN ISO 374-1, EN ISO 374-4 & EN ISO 374-5
  • This product is classified as 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)

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