Sterile White Nitrile 400 DI+

SHIELDskin Xtreme Sterile White Nitrile 400 DI+

Description | Features | Fact Sheets | Purchase Information 

Description

Powder Free Extra Length, extra DI washed Hand-specific Sterile 40cm Nitrile Gloves.  PPE Category III (Complex Design) according to Council Directive 89/686/EEC.  Fully compliant to the latest PPE norms - EN374:2003 “Protective gloves against chemicals and micro-organisms”.

Material

Synthetic soft nitrile polymer (Acrylonitrile Butadiene).  Contains no natural rubber latex.

Design

White, hand-specific, beaded cuff, with textured palm and fingers.

Packaging

Packaging designed to comply with sterile processing environments. Gloves pair packed in a sealed polyethylene pouch. Twenty (20) pouches per sealed (double) poly bag. Eight (8) poly bags per double- walled shipping case. Total of 160 pairs per outer case.

Quality Systems

Manufactured in accordance with ISO 9001:2000 and ISO 13485:2003.

Features

  • Biocompatibility demonstrated by Modified Buehler and Primary Skin Irritation Tests.
  • Non detectable levels of chemical allergens using aqueous solution extraction (Phosphate buffered solution) and High Performance Liquid Chromatography (HPLC) assay method for quantitative analysis.
  • Free of Thiurams and Thiazoles – these chemical accelerators are excluded from the manufacturing process.
  • Powder free to minimize the potential consequences of powder-borne dermatitis. Residual powder content is 1.0 mg/glove (typical) with a limit of 2.0 mg/glove (ISO 21171: 2006 “Medical gloves – Determination of removable surface powder”).
  • Micro-organism and virus resistant – passes highest level of micro-organism resistance per EN374-2: 2003 (Performance level 3, AQL <0.65 and inspection level G1 according to 1000ml water test) and passes viral penetration test using Phi-X 174 bacteriophage (ASTM F1671-97b).
  • Compatible with sterile processing environments due to paperless packaging and multiple post leaching of gloves.
  • Terminally sterilized by gamma irradiation to Sterility Assurance Level (SAL) of 10-6, in accordance with guidelines detailed in ANSI/AAMI/ EN ISO 11137:2006 “Sterilization of Healthcare Products – Radiation”.
  • Low Endotoxin content at <20 EU/pair (EN455-3:2006) demonstrated by Limulus Amoebocyte Lysate (LAL) kinetic turbidimetric test.
  • FTIR: non detectable levels of silicone, amide and DOP (IEST-RP-CC005.4).
  • NVR: maximum 30mg/g (IEST-RP-CC005.4). Extensively tested for chemical permeation according to EN374-3: 2003 (please refer to chemical resistance guide on website - www.shieldscientific.com/public/chemical-resistance-guide).

Fact Sheets

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Purchase information

ID

69 8771

Size

5.5

ID

69 8772

Size

6.0

ID

69 8773

Size

6.5

ID

69 8774

Size

7.0

ID

69 8775

Size

7.5

ID

69 8776

Size

8.0

ID

69 8777

Size

8.5

ID

69 8778

Size

9.0

ID

69 8779

Size

10