9
ENGLISH
NASAL ILLUMINATOR
Attach the Nasal Illuminator head to the handle by bayonet locking system, it is necessary to hold the battery handle
and nasal illuminator in each hand and match the bayonet grooves on both the nasal illuminator and handle, push
the head down and turn the head clock wise as in Fig.6.
Features
- Made from resilient thermoplastic material.
- Smooth and shiny surface ensure easy cleaning.
- Equipped with durable and easy locking system.
- Distal Fiber Optic illumination with super bright Xenon/Halogen Light.
- Easy replacement of lamp.
Changing the lamp
With the Otoscope, first unlock the head from the handle and pull the lamp (J) downwards as in Fig.7. Push in the
new lamp.
CLEANING AND STERILIZATION
The Nasal illuminator can be cleaned with a cloth moistened with Alcohol/IPA. This can be disinfected and sterilized
by any conventional method. Autoclaving is allowed (121°C).
Caution:
- Do not use the equipment in case it is damaged. Apply to your Retailer.
- Periodically check the battery conditions, making sure that no sign of corrosion or oxidation is present. In
case of necessity replace them with new ones.
- Carefully handle the batteries as the liquids can irritate skin and eyes.
- Before being used, thoroughly check the product. The same Operation shall be carried out after cleaning.
- Check that the connection between the head and the handle is perfect and that the On/Off Button works
correctly.
- If the light is intermittent or in case it does not turn on, check the bulb, the batteries and the electrical contacts.
Disposal: The product must not be disposed of along with other domestic waste. The users
must dispose of this equipment by bringing it to a specific recycling point for electric and elec-
tronic equipment.
GIMA WARRANTY TERMS
The Gima 12-month standard B2B warranty applies.
Caution: read instructions (warnings) carefully
Follow instructions for use
Keep in a cool, dry place
Keep away from sunlight
Manufacturer
Date of manufacture
Product code
Lot number
Medical Device compliant with Regulation
(EU) 2017/745
Type B applied part
WEEE disposal
Medical Device
