User's Manual
Table Of Contents
- 1. Warnings and precautions
- 2. Warranty conditions
- 3. The programmer system
- 4. The programmer tablet
- 5. The programmer software
- 6. The docking station
- 7. The inductive programming head
- 8. The radio frequency (RF) link
- 9. The ECG
- 10. The printer
- 11. Maintenance
- 12. Guidance and manufacturer's declaration
- 12.1. Radio equipment emission
- 12.2. Recommended separation distances according to the maximum output power of the communications equipment
- 12.3. Cable length
- 12.4. Electromagnetic emissions
- 12.5. Magnetic and Electromagnetic Immunity
- 12.6. Electromagnetic Immunity, Portable Radio Frequency Equipment
- 12.7. Raw materials
- 13. Technical data
- 13.1. Conformity of the programmer
- 13.2. US Federal Communications Commissions (FCC) and Industry Canada
- 13.3. Essential performances
- 13.4. Power supply
- 13.5. Dimensions programmer tablet
- 13.6. Dimensions docking station
- 13.7. Dimensions inductive programming head
- 13.8. Use constraints
- 13.9. Storage constraints
- 13.10. System specifications of the programmer
- 14. Explanation of symbols
- 15. Glossary
14. EXPLANATION OF SYMBOLS
General sym-
bols
Explanation of symbols
Manufacturer
Product reference number.
Product serial number.
Connector for a USB device.
Connector for an external
screen.
Connector for an Ethernet
LAN connection.
This symbol indicates the
minimum and maximum stor-
age temperature.
This symbol indicates the
minimum and maximum stor-
age humidity.
The product should be kept
dry.
This symbol indicates the
minimum and maximum stor-
age pressure.
The equipment contains con-
ductive parts and emits non
ionizing radiation (according
to standard IEC 60601-1).
This symbol concerns the in-
ductive programming head. It
indicates that this is BF Type
applied part, according to
standard IEC 60601-1 for
electrical medical equipment.
General sym-
bols
Explanation of symbols
Medical equipment with re-
spect to electric shock, fire,
and mechanical hazards, only
in:
― AAMI/ES 60601-1(2006)
/ A2 (2010) and
― CSA 22.2 NO 60601-1
CAN/CSA:2008.
Appropriate cables should be
used to avoid adverse effects
due to the possible discharge
of a cardiac defibrillator.
Magnetic Resonance (MR)
unsafe.
This electronic product is sub-
ject to disposal and recycling
regulations that vary by coun-
try and region.
Many countries prohibit the
disposal of waste electronic
equipment in standard waste
receptacles. For more details,
please refer to the European
Directive 2012/19/EU
(WEEE).
This symbol confers the ap-
proval of the US Federal
Communications Commis-
sion.
The device is compliant with
Japan’s radio standards.
The device is in full conformity
with European Directive
90/385/EEC.
Consult the documentation
and instructions for use.
Consult instructions for use
available on the company
website
www.microportmanuals.com.
14. EXPLANATION OF SYMBOLS
SmartTouch – UA10412A 33