Manufacturer Information; Automatic Shutdown - KCI ABThera Instrucciones De Uso

AC POWER / BATTERY
Power Cord
Unit should remain plugged into an AC power source while in use or in
• ABThera ™ (NPT)
storage to keep batteries charged.
• ABThera (NPT) Unit operates on an auto-ranging AC / DC power supply with a hospital
™
grade power cord.
• When fully charged the ABThera
™
maintain therapy during patient transport. Plug ABThera
source immediately after transport to maintain battery charge.
• When unplugged, ABThera (NPT)
™
intervention or therapy loss.
• Battery will fully recharge in approximately eight hours.

AUTOMATIC SHUTDOWN

While operating on battery power, if battery charge falls below a critical level (approximately
two hours or one hour after low battery alarm sounds) the ABThera
automatically turn off. When plugged into an AC outlet, the ABThera
Off until the Power On / Off button is pressed at which time therapy will resume (refer to
Keep Negative Pressure On under WARNINGS). See also Low Battery Alarm in the
Alarms section.
CARE AND CLEANING
Between patient use and if the product becomes soiled while in use in the hospital or other
healthcare organization, disinfectants containing quaternary ammonium compounds or
other similar disinfectant products may be used to clean the ABThera
organic material should be cleaned from the device prior to disinfection. Use personal
protective equipment (PPE) and hand hygiene protocols in accordance with local protocols
for cleaning and disinfection.
CAUTION: Avoid spilling fluid on any part of the ABThera
on electronic controls can cause corrosion which can cause the electronic components to
fail. Component failure may cause the ABThera
producing potential hazards to patient or care providers.
Battery Door
Unit will provide battery power in order to
(NPT)
power cord into an AC power
™
Unit will switch from AC to battery power without user
(NPT) Unit will
™
(NPT) Unit will remain
™
™ (NPT) Unit. All visible
(NPT) Unit. Fluids remaining
™
(NPT) Unit to operate erratically, possibly
™

MANUFACTURER INFORMATION

Manufactured for:
KCI USA, Inc.
San Antonio Texas, 78219
www.kci1.com
Do not use if package
is damaged or open
Single Use Only
Refer to Instruction
Manual
Not for regular waste
disposal
Type B applied
part
Sterilized with radiation
Rx only
Caution: Federal (USA) law restricts this device to sale by or on the order of a physician.
Dimensions
11.0 in H x 11.25 in L x 6.0 in D
27.94 cm x 28.6 cm x 15.2 cm
Weight
Therapy Unit only 5.7 lbs / 2.6 kg
Pressure options 100-150 mmHg, 13.3-20 kPa
Canister Volume 1000 cc / mL
Environmental Conditions
Storage Conditions
Temperature Range -20º F (-29º C) to 140º F (60º C)
Operating Conditions
Temperature Range 50º F (10º C) to 100º F (38º C)
Altitude Range
Optimum Performance 0 to 8,000 ft (0 to 2438 m)
* Specifications subject to change without notice.
7
KCI Medical Products (UK) Ltd.
Wimborne, Dorset, BH21 7SH
United Kingdom
www.kci-medical.com
SYMBOLS USED
Keep Dry Date of
Manufacture
Non Sterile Manufacturer
NON
STERILE
Use By
Authorized Representative
in the European
Community
Consult ETL Listed, Conforms to UL
i
Std. 60601-1 certified to
CM
Instructions
C US
CAN/CSA C22.2 Std. No.
for Use
3182664
601.1.
Biological Risk Conforms with the Medical
Device Directive (93/42/EEC)
0473 and has been subject to the
conformity procedures laid
down in the council directive
SPECIFICATIONS*
Electrical
Power Supply Input 100 V~ - 240 V~, 50/60 Hz
Power Supply Current 2.5 A max (100 V)
0.9 A (100 V~), 0.4 A (240 V~)
Current Leakage <100 Microamps (115 V)
<300 Microamps (230 V)
Battery Run Life 2 hours (approximately)
Battery Charge Time 8 hours (approximately)
IEC Classification
Medical Equipment
Equipment not suitable for use in presence of
flammable anesthetic mixture with air, oxygen or
nitrous oxide.
Type B Applied Part
IPX1