Technical Description Of The Medical Device; Control Unit - Comeg DUO Full HD Manuel D'utilisation

9 Technical description
of the medical device

Control unit

• Automatic white balance
• Video outputs:
- 1 HDMI
- 1 HD-SDI/3G-SDI
- 1 USB 3.0 micro B
• Compatible with Storz® and Olympus® type light
cables
• Electronic iris shutter
• Automatic thermal protection system
• Manual adjustment of the light intensity
• Anti-blinding feature with light cable detection
• LED technology
• LED lifetime up to 50 000 hours
• Color temperature: 5 400 K
• Intensity: max. 23 000 lux
• Brightness, detail, red and blue gains, color
adjustments
• Gain: Off / Low / High
• Freeze feature accessible from the camera head
• Flexible mode accessible from the control unit
and the camera head
• On screen displayed adjustments
• "SAVE" function to memorize the settings
• "RESET" function to restore to the factory settings
• Digital zoom up to 2.5x
• Full HD Images recorder integrated (USB) / .tiff
format
• Recommended USB stick format: FAT32
• Touchscreen with intuitive interface
• 17 languages
• Dimensions (W x H x D): 260 x 100 x 215mm
• Weight: 1900 g
• Protection type: IPX0 (not drip-proof)
• Power supply: 100 - 240 VAC / 50 - 60 Hz
• Power consumption: 85-95 VA
• Two T 1,6 A - 250 V fuses (Marked UL/CSA only)
• Continuous service
80
Camera head
• 1 CMOS Exmor RTMnology 1/2" Full HD
sensor
• 2 programmable buttons
• Automatic or adjustable electronic shutter
(1/50 to 1/100,000)
• Resolution: 1920 x 1080 p
• Definition: 1080 lines
• Active pixel area: 1920 x 1080
• Cable length 2.99 metres
• Dimensions (D x H): 130 x 47 mm
• Weight (camera only): 150 g
• Protection type: IPX7 (waterproof)
Lens (option)
• 24 mm HD lens
• C-mount, instrument holder with locking
mechanism
• Weight: 90 g
• Protection type: IPX7 (waterproof)
Environment
• Transport temperature: -10 °C / +45 °C
• Storage temperature: +10 °C / +40 °C
• Operating temperature: +10 °C / +40 °C
• Transport and storage relative humidity
between 20 and 85 %
• Operating relative humidity between 30 and
75 %
• Transport, storage and operating
atmospheric pressure : 700 hPa to 1060 hPa
• Electrical classification (IEC 60601-1): Class 1
• Type CF applied part
• Photobiological risk group (IEC 62471): Group
1
• This medical device complies with the
following international standards: IEC 60601-
1, IEC 60601-1-2, IEC60601-1-6, IEC 60601-
2-18, ISO 14971, ISO 15223-1, 62304, 62366
• Not suitable for use in the presence of a
flammable anaesthetic mixture containing
air, oxygen or nitrous oxide.