More Details

Construction:
* Two yarn ends of Dyneema
* Fibreglass wrapped in textured polyester.
* Cuff 5 knitted elasticised wrist

* Colour: White or grey
* Length: 229mm to 279mm
* Liner Material: Dyneema
* Sizes: 7, 8, 9, 10
* All ingredients conform to the applicable FDA indirect food additive regulations as prescribed by the FDA Code of Federal Regulations, Title 21, Part 177, Section 1520 'Olefin polymers' and Part 117, Section 2800 'Textile and textile fibres'

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Place Of Manufacture

Ansell Limited, Australia

Models

One model available in two colours:
* White: Style number 74-045, Sizes: 6,7,8,9,10,11 and Length:203-304mm
* Grey: Style number 74-047, Sizes: 6,7,8,9,10 and Length: 229-279mm

Maintenance

* Store in a cool dry area away from direct sunlight
* For detailed laundering instructions please contact Ansell Healthcare

Limitations of use
* Do not use near flames
* Do not use with temperatures greater than 70 degr C
* Do not use near moving or serrated blades
* Gloves are not puncture resistant

EN Chemical Hazard
* The gloves are not liquid proof, therefore do not use to protect against chemicals

Standards

Standards
Some assistive technology needs to meet Australian or other standards. Standards may relate to materials, manufacturing and installation. Products that meet Australian or international standards will have written certification. To find out if a product meets Australian Standards ask the supplier to show you the certificate. For more information about standards also see
http://at-aust.org/home/assistive_technology/standards.html

TGA
Many of the items on the Assistive Technology Australia website are categorised as a Medical Device. Medical devices that are approved for use in Australia have been entered into a national database called the Australian Register of Therapeutic Goods (ARTG), which is maintained by the Therapeutic Goods Administration (TGA). You can ask the supplier for the ARTG number for the device you wish to purchase and search the ARTG for the entry. To access information on the ARTG visit www.tga.gov.au

When buying a medical device it is advisable to only choose a medical device that is recommended by a healthcare professional and has been included on the ARTG.

Testing compliant to AS/NZS 2161
According to EN 388 (AS/NZS 2161.3:2005)