Otto Bock HealthCare MUG6081 Serial Cable Replacement User Manual UserMan
Otto Bock Healthcare Products GmbH Serial Cable Replacement UserMan
UserMan
GB
GB
BionicLinkModule
Printed in Austria - 11.05
The EUT is labled with its own FCC ID number. If the module is inside of an end product, the label will not be visible.
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The EUT is labled with its own FCC ID number. If the module is inside of an end product, the label will not be visible.
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Attention: To be installed by trained staff only.
1 Intended Use
The
BionicLinkModule
is used for a cordless configuration and diagnosis of other Otto Bock
products. Its main purpose is the replacement of the currently used serial cables. It has a
three wire serial interface.
2 Description and Function
It uses
Bluetooth
® technology, because this technology allows an easy connection to a PC,
a PDA or to a similar device. These devices either must have the Bluetooth® functionality
incorporated or use an external Bluetooth® interface such as a USB dongle or a Compact
Flash- or PC-Card.
The
BionicLinkModule
is conceived as a modular device, which can be permanently built
into other products of Otto Bock.
Special Features of the
BionicLinkModule
are:
•
The module is very flat.
•
Onboard PCB antenna, to achieve a higher antenna efficiency compared to the wide
spread ceramic antennas. The goal is to maximize the connection range without
increasing the output power of the RF components. This avoids unnecessary spurious
emissions and minimizes the power drain out of the battery of the prosthetic device.
•
One single LED indicator shows the user if the module is powered (LED is on) and if data
is transmitted (LED flashing).
3 Technical Data
Temperature Range:
0° - 60°C
Supply Voltage Range:
3.5 – 4.7V
Bluetooth Class II
4 Mounting Restrictions:
•
The module has to be mounted in a way to insure that the human tissue is held at a
minimum distance as shown in figure (2) and (3).
•
The module has to be placed isolated from metal surfaces at a minimum distance of
1mm, as shown in figure (1).
•
It is forbidden to make any modifications, especially of the antenna.
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Otto Bock Healthcare Products GmbH
Kaiserstraße 39 · 1070 Wien · Austria
Tel. (+43-1) 526 95 48 · Telefax (+43-1) 526 79 85
vertrieb.austria@ottobock.com · www.ottobock.at
Otto Bock has been
certified by the German
Society for the Certifi-
cation of Quality Assur-
ance Systems (DQS) in
accordance with DIN EN
ISO 9001, Reg. No. 779
( Management System).
This device complies with part 15 of the FCC Rules. Operation is subject to the following
two conditions:
(1) This device may not cause harmful interference, and
(2) this device must accept any interference received, including interference that may cause
undesired operation.
Modifications not expressly approved by Otto Bock could void the user’s authority to operate
the equipment.
NOTE:
This equipment has been tested and found to comply with the limits for a Class A
digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference when the equipment is operated in a
commercial environment.
This equipment generates, uses, and can radiate radio frequency energy and, if not installed
and used in accordance with the instruction manual, may cause harmful interference to
radio communications.
Operation of this equipment in a residential area is likely to cause harmful interference in
which case the user will be required to correct the interference at his own expense.
This product has a modular FCC approval according to FCC public notice DA 00-1407
(released: June 26
th
, 2000)
Industry
Canada
The EUT is labled with its own FCC ID number. If the module is inside of an end product, the label will not be visible.
Use only the supplied or approved antenna. Unauthorized antennas, modifi-
In this case the end product will be labled exterior with the following information:
cations or attachments could damage the terminal and may contravene
"This device contains FCC ID: SJ3MUG6081"
compliance. For portable applications OEM integrators need no SAR evaluation. The max source-based time-
local RF emission regulations or invalidate type approval.
OEM integrators and end-users must be provided with transmitter operating conditions for satisfying RF exposure
End users may not be provided with the module installation instructions.
averaged output of 0.5 mW is below the low threshold of 24mW for d < 1.5 cm.