USER and MAINTENANCE MANUAL
6110 A1 and 6110 A2
Manufacturer: Siem Nova S.r.l. Legal and operational offices Via C. Varalli, 1 20087 ROZZANO (Milano) MADE IN ITALY
Product: SURGICAL ASPIRATOR MOD:
6110 A1 MAX - 6110 A2 SPEEDY
Updated: 2018-01-09
reproduction forbidden
Pag: 9 di 10
The 6110-A1 and 6110-A2 equipments are protected against the penetration of liquids and solids (IP33) It
is always good though protect from heavy rains. During operation and storage, the device should be kept dry. If the
device is entirely wet, move it to a dry area, dry externally and wait at least 30 minutes before using it again if you
are sure that water didn’t enter inside.
REMARKS: The suction equipments could be equipped with two different pumps (120l/min or 90 l/min)
6110-A1 MAX and 6110-A2 SPEEDY equipped with 120 L/min pump
Dimensions (h x w x l):
965 x 400 x 330 mm (38 x 15,7 x 13 inches)
Voltage with motor HP 120:
230 VAC; 50 Hz; 325 VA
Operating cycle:
continuous
flow rate (before the filter):
> 120 liters/minute (+/– 5 %) with motor HP 120
Standard Canister volume:
2000 ml
weight (without canister):
22 kg / 48,5 lbs approx
max. vacuum level:
– 697,5 mmHg / – 93 kPa /- 0,93 bar (+/- 5 %) (*)
CEI EN60601-1 Classification:
Insulation Class I device - Applied part type B
Device not suitable for use in presence of flammable anesthetic mixture with air,
oxygen or nitrogen protoxid.
UNI EN ISO10079-1 Classification:
Equipments with HIGH VACUUM level and HIGH FLOW
DDM 93/42 CEE Classification:
Class ll b
6110-A1 MAX and 6110-A2 SPEEDY equipped with 90 L/min pump
Dimensions (h x w x l):
965 x 400 x 330 mm (38 x 15,7 x 13 inches)
Voltage with motor HP 90:
230 VAC; 50 Hz; 270 VA
Operating cycle:
continuous
flow rate (before the filter):
> 90 liters/minute (+/– 5 %) with motor HP 90
Standard Canister volume:
2000 ml
weight (without canister):
20 kg / 48,5 lbs approx
max. vacuum level:
– 675 mmHg / – 90 kPa- 0,9bar (+/- 5 %) (*)
CEI EN60601-1 Classification:
Insulation Class I device - Applied part type B
Device not suitable for use in presence of flammable anesthetic mixture with air,
oxygen or nitrogen protoxid.
UNI EN ISO10079-1 Classification:
Equipments with HIGH VACUUM level and HIGH FLOW
DDM 93/42 CEE Classification:
Class ll b
(*) Measured at 0-meter, atmospheric pressure: 1013.25 hPa.
PLEASE NOTE: vacuum levels may vary depending on location (meters above sea level, atmospheric
pressure and temperature).
10 DISPOSALS
At the end of their operative life the device and accessories must be disposed of in compliance with the local regulation and
enviromental laws, if no legal regulation exists the different material must be sorted and disposed of separately (see the below
table)
Remark: the components of the equipments or accessories don’t contain phthalates or natural latex
Item
Material or regulation
Suction pump unit and power cord
Waste from Electric and Electronic Equipment (WEEE)
Unit case
NON-MAGNETIC ALUMINIUM frame
Canister
Polycarbonate
Lid
Polycarbonate
Rubber components
Silicone
Cage and float
Polypropilene
box
Cardboard
manual
Paper
Remark: the components of the equipments or accessories don’t contain phthalates or natural latex
11 ELECTROMAGNETIC COMPATIBILITY
The suction pump 6110-A1 AND 6110-A2 are supplied with an electric induction motor and has no electronic parts so for his own
nature he doesn´t generate electromagnetic emissions or is influenced by external electromagnetic emissions , to this means that
this device is automatically in compliance with the requirements of CEI EN 60601-1-2-2015 for the electromagnetic compatibility of
medical devices, anyhow the use of mobile telephones, LAN / WLAN, walkie-talkies (two-way radios) and cordless telephones sets
could affect the 6110-A1 AND 6110-A2 pump. A safety distance of min. 3.3 ft (1 m) to the equipment is recommended.
