General Warning; Important Safety Rules; Technical Characteristics - Gima 28220 Manual De Instrucciones

7
TOBI MANUALE SUCTION ASPIRATOR it's a manual device to be used for the emergency field to be used
for the aspiration of the body liquids (mucus or catarrh or blood). Easily movable and designed for a manual
use. Thanks to this characteristics and to the rating that it has product is particularly suitable for a emergency
use, on the thacheotomized patients, minor surgical applications and post - operative therapy at home. Made
of highly heat resistant, in conformity with the latest European safety standard, the product is supplied with a
polycarbonate 0.4 litre autoclavable jar with overflow valve.

GENERAL WARNING

Read instruction manual carefully before use.
Only highly qualified staff use reserved the instrument must not disassembled.
For technical service always contact Gima S.p.A.

IMPORTANT SAFETY RULES

1. Check the condition of the unit before each use.
2. Respect the safety regulations indicated for electrical appliances and particularly:
- Use original components and accessories provided by the manufacturer to guarantee the highest effi-
ciency and safety of the device;
- The device can be used only with the bacteriological filter;
- Place instrument on stable and flat surfaces;
- Don't touch the device with wet hands and always prevent the appliance coming into contact with liquids;
- Keep off the reach of children or not capable people without supervision;
- Preserve and use the medical device in environments protected from atmospheric factors and at distance
from heat sources;
- Don't use the device thoracic drainage.
3. For repairs, exclusively contact technical service and request the use of original spare parts. Failure to
comply with the above can jeopardise the safety of the device.
4. Use only for the purpose intended. Don't use for anything other than the use defined by the manufactur-
er. The manufacturer will not be responsible for damage due to improper use.
5. Instrument and accessory discharging must be done according to current regulations in the country of use.
6. None of mechanical parts have been designed to be repaired by customers or end-users. Don't open the
device, do not mishandle the mechanical parts. Always contact technical assistance.
7. Using the device in environmental conditions different than those indicated in this manual may harm seri-
ously the safety and the technical characteristics of the same.
The manufactured cannot be held liable for accidental or indirect damages should the device be mod-
ified, repaired without authorization or should any of its component be damaged due to accident or misuse.
Any minimal modification / repair on the device voids the warranty and does not guarantee the compliance with
the technical requirements provided by the MDD 93/42/EEC (and subsequent changes) and its normatives.

TECHNICAL CHARACTERISTICS

Model
TIPOLOGY (MDD 93/42/EEC)
Classification UNI EN ISO 10079-2
Maximum suction aspiration (without jar)
Weight
Dimension
Working condition
Conservation condition
ENGLISH
TOBI MANUALE SUCTION ASPIRATOR
Medical Device Class IIa
MEDIUM VACUUM / 22l/min
-40kPa (- 0.40 bar)
1.150 Kg
225 x 165 (h) x 85 mm
Room temperature: 5 ÷ 35°C
Room humidity percentage: 30 ÷ 75% RH
Altitude: 0 ÷ 2000m s.l.m
Room temperature: - 40 ÷ 70°C
Room humidity percentage: 10 ÷ 100% RH