SHIELDskin Xtreme Sterile Latex 330 DI+

SHIELDskin Xtreme Sterile Latex 330 DI+

Description | Features | Fact Sheets | Purchase Information 

Description

Powder Free Extra Length, extra DI washed Hand-specific Sterile 33 cm Natural Rubber Latex 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

Natural Rubber Latex. Contains 50 micrograms or less of total water extractable protein per gram, using the EN455-3: 2006/ ASTM D5712-05 Modified Lowry Method.  Typical measurements for latex protein are ≤30µg/g as per Modified Lowry Method.

Design

Natural colour, hand-specific, beaded cuff and textured palm.

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 Thiazole free – these chemical accelerators are excluded from the manufacturing process. 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).
  • 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”).
  • 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.
  • 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

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Purchase information

ID

69 5761

Size

5.5

ID

69 5762

Size

6.0

ID

69 5763

Size

6.5

ID

69 5764

Size

7.0

ID

69 5765

Size

7.5

ID

69 5766

Size

8.0

ID

69 5767

Size

8.5

ID

69 5768

Size

9.0

ID

69 5769

Size

10