Invacare Octave User manual

User Manual (EN)
Invacare®OctaveTM

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Table of Contents
1. General Information ......................................3
2. Operating the OctaveTM ....................................7
3. Receiving the OctaveTM....................................11
4. Disassembly of parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
5. Wiring .................................................15
6. Part numbers for accessories ..............................16
7. Cleaning and Maintenance.................................17
8. Trouble-shooting the electrical system ......................20
9. Electrical data ...........................................21
10. Technical specifications ..................................25
11. Weight................................................27
12. Disposal ...............................................27

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QA XXX
EN
1. General information
This manual must be given to the user of the product. Before using this product, read this manual and save for
future reference.
Please note that there may be sections in this User Manual, which are not relevant for your bed.
All indications of right and left are based on a patient lying on his back in the bed.
Metal side rails and U-profile bed ends may be disassembled without the use of any tools.
1.1 Intended use
 The bed is designed for use especially for home care.
 The bed is designed for patients over the age of 12 years. 150 cm and longer.
 The bed is a nursing bed with modular structure.
 Max patient weight: 350 kg (provided the equipment - bed ends, side rails, support handles, lifting pole and
mattress have a total weight of max 35 kg).
 Safe Working Load: Max 385 kg (Patient + accessories).
 The Ocatve™ bed is defined to be used according to;
Application environment 3;Long-term care in a medical area where medical supervision is required and
monitoring is provided if necessary and medical electrical equipment used in medical procedures may be pro-
vided to help maintain or improve the condition of the patient.
Application environment 4; Care provided in a domestic area where medical electrical equipment is used to
alleviate or compensate for an injury, disability or disease.
In order to optimise the patient’s comfort Invacare® recommends using a 15 cm mattress.
(see order numbers in section 6 "Part numbers for accessories").
1.2 Certification
 OctaveTM is marked in accordance with directive 93/42/EEC concerning Medical
Devices.
 OctaveTM is tested and approved in accordance with EN 60601-2-52 of TÜV
Product Service in Germany.
 OctaveTM has undergone a risk analysis according to EN 14971.
 The motors and control unit of the bed are approved according to IEC 60601-1:2005 3:rd edition.
The hand control, control unit and motors are protected according to IPX6 or IPX4.
A lock cam must be used on the control unit - if not, Invacare®can not guarantee the IP protection.
All service work described in chapter 7 may only be performed by personnel who have been trained or instructed
by Invacare® service course.
If the functions of the bed change, please send the bed for a check-up according to the maintenance chart in
chapter 7.
Invacare® is certified according to EN ISO 9001 and ISO 13485 and ensures compliance by 3:rd party.
Throughout the entire production process our materials/products are quality controlled by the operators.
Additionally, a final test is carried out prior to packaging and shipping.
The operator carrying out the final test, which includes a check of all moveable
parts, motors and castors, issues a QA number on the product thereby confirming
its quality.
If the product does not correspond to the quality demands of Invacare®, it will be discarded.
If, contrary to our expectations, a problem should arise in connection with the delivered product, please contact
your Invacare® supplier. An address list is shown on the back of this manual.

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1.3 Labels and symbols
Symbols in this user manual:
WARNING
Indicates a hazardous situation that could result in serious injury or death if it is not avoided.
INFORMATION
Gives useful tips, recommendations and information for efficient, trouble-free use.
Maximum user weight
Safe working load (SWL) (Patient + mattress + side
rails + lifting pole + other equipment).
This product complies with Directive 93/42/EEC concerning medical devices.
The launch date of this product is stated in the CE Declaration of conformity.
The product should be reused
where possible
Applied Part, Type B, complying
with the specified requirements
for protection against electrical
shock according to IEC60601-1.
(An applied part is a part of the
medical equipment which is
designed to, or are likely to, come
into physical contact with the
patient.
INSTRUCTION
Reference to the user manual.
Labels / symbols on the product:

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EN
Date of production. Symbols
Electrical information
Type no. of the bed.
Serial no.
To identify the product please look at the product label:
IPX4 or IPX6 depend-
ing on configuration.
Back rest
Seat section
Leg section
Thigh section
1.4 Description of the main parts in the mattress support:
Iin Current in
Vin Voltage in
Int. Intermitens
AC Alternating current
Max Maximum
min minutes
kg kilogram
A Ampere