User's Manual
Table Of Contents
- 1.Introduction
- 2.Product Description
- 3.Indications for Use
- 4. Package Contents
- 5. Features and Benefits
- 6.Specifications
- 7.Operating Procedure
- 7.1 Product indication and key function
- 7.2 OLED screen description
- 7.3 Specific operation method
- 8.Changing the O-Ring
- 9.Attention
- 10.FCC Caution
- 11. Device Label
- 12.Label Symbols Defined
- 13.Prevention of Cross-Contamination
- 14.Troubleshooting
- 15.Manufacturer Warranty, Service and Support
- 16.Magnetic compatibility information
- Guidance and manufacturer´s declaration – electrom
- Guidance and manufacturer´s declaration – electrom
Min I(Smart) User Manual
12
Guidance and manufacturer's declaration – electromagnetic immunity –
for all EQUIPMENT and SYSTEMS
Guidance and manufacturer's declaration – electromagnetic immunity –
for all EQUIPMENT and SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic emission
The Mini I(Smart I) Electric Oral Anesthesia Injector is intended for use in the electromagnetic environment specified
below. The customer or the user of Mini I(Smart I) I Electric Oral Anesthesia Injector should assure that it is used in
such an environment.
Emissions test
Compliance
Electromagnetic environment - guidance
RF emissions
CISPR 11
Group 1
The Mini I(Smart I) Electric Oral Anesthesia Injector uses RF energy
only for its internal function. There for, its RF emissions are very low
and are not likely to cause any interference in nearby electronic
equipment.
RF emissions
CISPR 11
Class B
The Mini I(Smart I) Electric Oral Anesthesia Injector suitable fo
r use in allestablishments,
including domestic establishments and those directly connected to
the public low-voltage power supply network that supplies
buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
N/A
Voltage fluctuations
flicker emissions
IEC 61000-3-3
N/A
Guidance and manufacturer´s declaration – electromagnetic immunity
The Mini I(Smart I) Electric Oral Anesthesia Injector is intended for use in the electromagnetic environment specified
below. The customer or the user of the Mini I(Smart I) Electric Oral Anesthesia Injector should assure that it is used in
such an environment.
Immunity test
IEC 60601
test level
Compliance level
Electromagnetic environment -
guidance
Electrostatic
discharge (ESD)
± 8 kV contact
± 2 kV, ± 4 kV, ± 8 kV,
± 8 kV contact
Floors should be wood, concrete or
ceramic tile. If floors are covered with