CHECK MOISTURE
– indicates that moisture or exudate has been detected in the power unit. The power unit will
cease to operate on this indication. Refer to Direct Healthcare Group for service assistance.
If any of the following faults are displayed the power unit will cease to operate:- PUMP OPEN; NO CANISTER; PUMP
OFF FAULT (PUMP SHORT); RELEASE KEY; BATTERY FAULT. Should any of these faults occur, press the MUTE button
to reset the power unit. If fault remains/re-occurs, contact Direct Healthcare Group.
The power unit may also display the following information (the power unit will continue to run whilst these messages
are displayed):-
• SERVICE DUE - Contact Direct Healthcare Group to arrange service
• UNCALIBRATED - Contact Direct Healthcare Group for recalibration.
8. Technical Specifications
8.1 VENTURI COMPACT Power Unit
[Medical Device Classification: Class IIb - conforms with Directive (93/42/EEC) Annex II (excluding Section 4)
Model Ref.:
Venturi v.II TG600/08
Construction:
Flame retardant ABS
Dimensions:
W161mm/6.3” x H155mm/6.1” x D90mm/3.5”
Weight:
1.0kg / 2.2 lbs
DC Input Voltage:
12V Nominal
Vacuum Application:
Continuous (default therapy) or intermittent
Pressure Range:
10 to 180mmHg (+0mmHg / -20mmHg)
Fixed Internal Battery: 3.7V 10Wh Lithium Ion Rechargeable Cell
IP Rating:
IP22
Noise Level:
43 dBa
8.2 Canister
(ACCESSORY to TG600/08)
Construction:
ABS, textured (includes desiccant)
Capacity:
300 ml
Dimensions:
W156mm/6.1” x H163mm/6.4” x D32mm/1.3”
8.3 Power Adapter
(ACCESSORY to TG600/08)
Mains Adapter Type:
FW7556M/12 / VEP15US12 (supplied)
Input:
100-240V / 50-60Hz / 400mA
Output:
12V dc / 1.5A
Cable Length:
4 metres / 13’
Part Number:
10245
The above mains adapters are considered part of the ME equipment.
The
VENTURI
COMPACT power unit must only be used with the specific external power adapter as supplied by Direct
Healthcare Group.
EXPECTED SERVICE LIFE: The expected service life of the medical device and its ACCESSORIES is five years.
SPECIFIED SHELF LIFE: The product has no specified shelf life.
Products are free from TSE species derived materials, medicinal substances, human blood derivatives and phthalates.
Talley manufacture products to comply with National and International safety standards and are certified to ISO13485,
Medical Devices Directive 93/42/EEC and Medical Device Regulation 2017/745.
D H G - H E A LT H C A R E . C O M
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