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GE Vivid E7 User Manual

GE Vivid E7
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GE
D
IRECTION GB091046, REVISION 2 VIVID E9 / VIVID E7 BT’13 SERVICE MANUAL
1 - 8 Section 1-3 - Important conventions
1-3-3 Product icons
The following table describes the purpose and location of safety labels and other important information
provided on the equipment.
Table 1-6 Product icons sheet 1 of 4
LABEL/SYMBOL PURPOSE/MEANING LOCATION
Identification and Rating Plate
- Manufacturer's name and address
- Date of manufacture
- Model and serial numbers
- Electrical ratings
Rear of console near power inlet
Type/Class Label
Used to indicate the degree of safety or
protection.
Rear of console
Equipment Type BF (man in the box
symbol) IEC 878-02-03 indicates B Type
equipment having a floating applied part.
Probe connectors including Doppler probe
connector
Equipment Type CF (heart in the box
symbol) IEC 878-02-05 indicates
equipment having a floating applied part
having a degree of protection suitable for
direct cardiac contact.
Probe connectors and ECG connector.
On newer systems also on the rear of the
system.
DEFIBRILLATOR-PROOF TYPE CF
EQUIPMENT.
At the ECG connector on front of system.
Device Listing/Certification Labels
Laboratory logo or labels denoting
conformance with industry safety
standards such as UL or IEC.
Rear of console
“CAUTION - This unit weighs … Special
care must be used to avoid …”
This precaution is intended to prevent
injury that may result if one person attempt
to move the unit considerable distances or
on an incline due to the weight of the unit.
On the console where easily seen during
transport
Do not push VIVID E9 / VIVID E7
sideways when casters are in break
position. Instability may occur.
Both sides of Top Console
“DANGER - Risk of explosion used in…”
The system is not designed for use with
flammable anesthetic gases.
Rear of console

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GE Vivid E7 Specifications

General IconGeneral
BrandGE
ModelVivid E7
CategoryMedical Equipment
LanguageEnglish

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