2
Electronic Thermometer
3000
AD/ADA
•
15, 30, 45 and 60 second pulse Timer
•
Easily accessible probe cover box
•
Easy to read LCD display with backlight
•
Cold Mode – lower pre-heat temperature option provides quicker, accurate readings for post-OR patients
•
Theft prevention lock out and anti-theft accessories
iii. safeTy and WarninGs
Caution: Federal law (USA) restricts this device to sale by or on the order of a physician.
1. Read this booklet thoroughly before using the FILAC 3000 electronic thermometer.
2. Do not use this device near flammable anesthetics. Not suitable for use in the presence of flammable anesthetic mixture with air,
oxygen or nitrous oxide.
3. Do not use this thermometer without first installing a new FILAC 3000 electronic thermometer probe cover.
4. Use only FILAC 3000 electronic thermometer probe covers
with
this device.
Use of any other probe cover will result in erroneous temperature readings.
5. The device and probe covers are Non-sterile. Do not use on abraded tissue.
6. To limit cross contamination, use Blue devices for Oral and Axillary temperature taking only.
7. Use RED devices only for RECTAL temperatures.
8. Thoroughly dry all electrical contacts on both probe and thermometer after washing, or device may fail to function properly.
9. For re-calibration, service or integrity checks, refer to a qualified Biomedical Technician or return to manufacturer.
10. Do not open unit. No user-serviceable parts inside. Opening of device may affect calibration and voids warranty.
11. Disposal of used probe covers must be performed in accordance with current medical practices or local regulations regarding
disposal of infectious, biological medical waste.
12. Removal of the batteries is recommended if the unit is not going to be used for an extended period of time.
13. Dispose of batteries in a manner consistent with local environmental and institutional policy for Lithium or Alkaline battery
disposal.
14. Dispose of old battery-powered electronic equipment in a manner consistent with institutional policy for expired equipment
disposal.
15. Cleaning frequency and practices must be consistent with institutional policy for cleaning of non-sterile devices.
16. Device to be used by trained personnel.
noTe
:
Even though this device has been designed to minimize the effects of electromagnetic interference, it does generate radio frequency
energy. If not used in accordance with the instructions, the device could cause interference in other equipment operating within its
vicinity. If the device is causing interference, the following actions may be taken in an attempt to correct the interference:
• Re-orient or re-locate the receiving device.
• Increase the separation between the devices.
• Consult a customer service representative.
iV. iCon idenTifiCaTion
See Accompanying
Documents
Manufacturer Serial Number
Type BF Equipment
Degree of protection against
electrical shock – no conductive
connection to the patient
Date of Manufacture
EN 50419
