User's Guide
Table Of Contents
- 1 Welcome!
- 1.1 Use specification
- 1.2 About the Demetra solution
- 1.3 What’s in the box
- 1.4 Demetra Scope
- 1.5 Demetra Web Application
- 2 Installation and configuration
- 2.1 Setup of Demetra Web Application
- 2.1.1 Minimum system requirements
- 2.1.2 Activation
- 2.1.3 Configuration (admin)
- 2.1.4 Configuration (user)
- 2.1.5 Settings
- 2.2 Installation of Demetra Scope
- 2.2.1 Installation of the grip / battery pack
- 2.2.2 Removal of the grip / battery pack
- 2.2.3 Installation of the non-contact cone
- 2.2.4 Charging the Demetra Scope
- 2.3 Setup of Demetra Scope
- 2.3.1 Configuration
- 2.3.2 Status bar
- 2.4 When the Demetra subscription is terminated
- 3 Operation with the Demetra Scope
- 3.1 Start the Demetra Scope
- 3.2 Basic workflow
- 3.3 Live video preview
- 3.4 Image detail screen
- 3.5 Localize (on clinical overview)
- 3.6 Diagnose
- 4 Operation with the Demetra Web Application
- 4.1 Open the Demetra Web Application
- 4.2 Main menu
- 4.3 Patient detail screen
- 4.4 Consultations screen
- 4.5 Image detail screen
- 4.6 Diagnose
- 4.7 Reports
- 5 Troubleshooting
- 5.1 Troubleshooting instructions
- 6 Repacking instructions
- 6.1 Repacking overview
- 7 Cleaning and disinfection
- 7.1 Instructions
- 8 Important information
- 8.1 Safety information
- 8.2 Environmental information
- 8.3 Regulatory compliance information
- 8.3.1 EU statement
- 8.3.2 FCC statement
- 8.3.3 Industry Canada statement - Avis d'industrie Canada
- 8.3.4 General information
- 8.4 EMC notice
- 8.5 Explanation of symbols
- 8.6 Explanation of icons
- 8.7 Legal disclaimer
- 8.8 Technical specifications
K5902200 /02AC Barco Demetra 51
Indicates compliance with Part 15 of the FCC rules
Indicates the device is approved according to the UL regulations
MEDICAL – GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE
AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH ANSI/AAMI ES
60601-1 (2005) + AMD (2012) and CAN/CSA-C22.2 No. 6060-1 (2014)
Indicates the device is approved according to the UL regulations for Canada and US
E352529
Indicates the device is approved according to the UL regulations for Canada and US
Indicates the device is approved according to the UL Demko regulations
S&E
Indicates the device is approved according to the CCC regulations
Indicates the device is approved according to the VCCI regulations
Indicates the device is approved according to the KC regulations
Indicates the device is approved according to the BSMI regulations
Indicates the device is approved according to the PSE regulations
Indicates the device is approved according to the EAC regulations
Caution: Federal law (United Stated of America) restricts this device to sale by or on
the order of a licensed healthcare practitioner.
Indicates the USB connectors on the device
Indicates the DisplayPort connectors on the device
Type BF applied part
Class II equipment
Important information