Active Design CAPS II - Important Information; Statutory Compliance; Testing; Warranty

INS150 Version 1
29
November 2018
7
Important Information
7.1
Statutory Compliance
Our seating systems are manufactured to comply with the Medical Devices
Directive MDD93/42/EEC and amendments in 2007/47/EEC. In terms of the
Medical Devices Directive, our seating systems are classified as Class I Medical
Devices.
7.2
Testing
7.2.1
Fabric
We need our fabrics to last. We independently test the materials used in our
seating systems to the following standards:
• BS EN ISO 105-C06:1997 (Colour fastness)
• BS EN ISO 105-BO2:1999 (Fastness to light)
• BS EN ISO 12947-2:1998 Martindale abrasion resistance (30000 rubs with
12kPa load)
7.2.2
Foam
Our Reflex foams are tested to:
• BS 5852-2:1982 using Ignition Source Crib 5
7.2.3
Actiflex
The fabric used in our Actiflex lap straps and harnesses has been tested to the
Aerospace standard C525.853 Part 1 Appendix F a-I for flammability.
7.3
Warranty
All of our products are manufactured to the highest standards.
Active Design offers a two year warranty against defects in material and
workmanship from the date of purchase. Active Design will not be held responsible
for any damage or injury due to misuse or modifications of these products.