Intended Use; Scope Of Delivery; User Manual - Invacare Aquatec Dot Manuel D'utilisation

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  • FRANÇAIS, page 6
Aquatec® Dot
Fig. 3
Fig. 5
1.2 Symbols in this user manual
In this user manual, warnings are marked with symbols. The title next
to the warning symbol indicates the level of danger.
WARNING
Indicates a dangerous situation which could lead to
death or serious injury if not avoided.
CAUTION
Indicates a dangerous situation which could lead to
minor injuries if not avoided.
IMPORTANT
Indicates a dangerous situation which could lead to
damage if not avoided.
Useful tips, recommendations and information to
ensure efficient and smooth operation.
This product complies with the directive 93/42/EEC
for medical products. The launch date for this product
is specified in the CE declaration of conformity.
Manufacturer

1.3 Intended use

The shower stool is to be used solely as an aid for sitting in the
bathroom or in the shower for people with sufficient torso stability.
Any other use is prohibited.
Operating temperature: 10 – 40 °C
2
F
B
D
Fig. 4
Fig. 6

1.4 Scope of delivery

The following components are included in the scope of delivery (Fig.
1):
A
Seat plate
B
Height adjustable legs (4x) composed of two into each other
moveable tubes, clips and rubber tips
C

User manual

1.5 Warranty
We provide a manufacturer's warranty for the product in accordance
with our General Terms and Conditions of Business in the respective
countries. Warranty claims can only be made through the provider
from whom the appliance was obtained.
Quality
Quality is of the utmost importance for our company; all processes
are based on the ISO 9001 and ISO 13485 standards.
This product features the CE mark, in compliance with the Medical
Device Directive 93/42/EEC Class 1.
The product meets the requirements of the standards DIN EN 12182
(Technical aids for disabled persons - general requirements and test
methods), DIN EN ISO 14971 (Medical devices - Application of risk
management to medical devices) and DIN EN ISO 10993–1 (Biological
evaluation of medical devices - Part 1: Evaluation and testing within a
risk management system).
C
1563094-B

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