Daavlin 1 Series Kullanım Kılavuzu - Sayfa 7
Tıbbi Ekipman Daavlin 1 Series için çevrimiçi göz atın veya pdf Kullanım Kılavuzu indirin. Daavlin 1 Series 19 sayfaları. Modes of operation - timed mode
Sayfayı Yazdır•
All treatments must be administered under the direction of a licensed physician only.
•
Device is not to be used in MR environments that may include MRI, diathermy, electrocautery,
or other high frequency equipment.
•
Do not treat if the lamps fail to ignite. Consult with doctor and/or contact Daavlin customer
service. (See page 21)
•
If lamps turn on without treatment being started/resumed, or if lamps do not turn off when
treatment is completed, unplug the device. Contact doctor and/or Daavlin customer service.
(See page 21)
•
DT
Phototherapy Devices are considered CISPR Group 1, Class A devices, to be
Controlled
used for prescription use only.
8.0 Operating Specifications
Ambient
Temperature:
Relative Humidity:
Liquid Ingress
Rating:
Ocular Hazard
Distance:
Ambient
Luminance:
WARNING: Equipment not suitable for use in the presence of a flammable anesthetic mixture
with air or with oxygen or nitrous oxide.
9.0 Labels and Symbols
If the unit is equipped with FlexRx™ exposure limiting software, there will be a label similar to the
one shown below (Figure 1 FlexRx Label) below informing you that your unit has been equipped
with this feature.
MNL-00049 [1]
15°C to 30°C (59°F to 86°F)
10% to 95%, Non-condensing
IPX0 (This device does not have protection
against ingress of water.)
3 Meters (9.84 Feet)
250 – 500 lux
Figure 1 FlexRx Label
Proprietary and Confidential. Printed copies will not be updated.
Page 7 of 19