Sterile White Nitrile 330 DI+

Description | Features | Fact Sheets | Purchase Information 

Description

Powder Free Extra Length DI washed Hand-specific Sterile 33cm 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), based on Skin Nitrile™ technology. 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. Ten (10) poly bags per double- walled shipping case.  Total of 200 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 accelerators using aqueous solution extraction (Phosphate buffered solution) and High Performance Liquid Chromatography (HPLC) assay method for quantitative analysis.
• Thiuram and Dithiocarbamate free – 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 “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).
• 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”.
• Compatible with sterile processing environments due to paperless packaging and multiple post leaching of gloves.
• NVR: maximum 30mg/g (IEST-RP-C0005.3).
• FTIR: non detectable levels of silicone, amide and DOP (IEST-RP-C0005.3).
• Low Endotoxin content at <20 EU/pair (EN455-3:2006) demonstrated by Limulus Amoebocyte Lysate (LAL) kinetic turbidimetric test.

Fact Sheets

Purchase information