MEDLINE HEMO-FORCE LITE Intermittent DVT Pump User Manual

MDS600INTHL
HEMO-FORCE LITE Intermittent DVT Pump
User Manual

INTRODUCTION

The Hemo-Force is an Intermittent Pneumatic Compression System that counteracts blood stasis and coagulation changes; two of the three major factors that promote deep vein thrombosis (DVT) a potentially life-threatening condition which can lead to pulmonary embolism.
The Hemo-Force is a non-invasive mechanical prophylactic system that massages the feet or legs in a wavelike, milking motion that promotes blood flow and deters thrombosis, helping to empty pooled or static blood from the valve cusps of the femoral vein. Fibrinolytic activity is increased, stimulating the release of a plasminogen activator. This therapy typically complements other prophylactic measures, such as antiembolic stockings and anticoagulants.
Some exciting features include:

• User friendly master control unit that is designed so that its functions are self-explanatory
• Power micro switch (ON/OFF)
• An alarm light displays a fault status with an audio alarm and LED display
• LED display that can monitor errors and sleeve type of the device
• User friendly hanging bracket that provides easy attachment

INTENDED USE

The system consists of an air pump and single-patient-use compression sleeves – one for the foot, one for the calf and one for the thigh. The air pump and compression sleeve may be used on one lower extremity. If the air pump is used simultaneously on both lower extremities, it is important that the identical sleeve type be used on both legs (i.e. foot sleeve with foot sleeve, calf sleeve with calf sleeve, or thigh sleeve with thigh sleeve). The inflation pressure settings are pre-set by the manufacturer and cannot be changed. The compression level for the foot sleeve is 120mmHg (16kPa). The compression level for the calf and thigh sleeve is 40mmHg. The sleeve inflates and maintains compression for 12 seconds. Then, the sleeve deflates for a period of 48 seconds. As the sleeve inflates, it compresses the foot, calf or thigh which augments venous blood flow, thereby reducing stasis. This process also stimulates fibrinolysis; thus, reducing the risk of early clot formation. Regularly check the system while in use, assuring pump operation and sleeve fit.
Please note: It is NOT RECOMMENDED that patients with the following conditions use this product without consulting with a physician.

CONTRAINDICATIONS

The use of the Hemo-Force Lite is NOT RECOMMENDED in the following conditions:

1. Severe congestive cardiac failure
2. Severe arteriosclerosis, thrombophlebitis or other ischemic vascular disease
3. Extreme deformity of the limbs
4. Known or suspected deep vein thrombosis
5. Known or suspected pulmonary embolism
6. Any local condition in which the sleeve would interfere: i.e.
   a. Gangrene
   b. Dermatitis
   c. Untreated or infected wounds
   d. Recent skin grafts

WARNINGS AND CAUTIONS

1. Keep the pump and sleeve away from sources of liquid and open flames.
2. Keep the pump and sleeve away from sharp objects.
3. If pain, irritation, numbness, swelling, or redness occurs discontinue use and contact a healthcare professional.
4. The Pump should always be used in conjunction with hospital policy.
5. The Pump should only be repaired by an authorized professional.
6. Do not drop the control unit or store it in direct sunlight or extreme cold conditions.
7. Do not use the system in the presence of any flammable gases (such as Anaesthetic Agents).
8. Connect the Master Control unit to an adequate power source.
9. No modification of this equipment is allowed.
10. Power cable & pump shall be placed at the foot-side of the patient to prevent any risk of strangulation due to cable.
11. Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
12. This device can be used in home healthcare and professional healthcare environment.
13. This device should not be used adjacent to or stacked with other equipment.
14. Medical electrical equipment needs special precautions regarding EMC and needs to be installed according to the EMC information provided.
15. Please ensure the pump is used with stable power or in connection with UPS (Uninterruptible Power Supply).

CAUTIONS
Do not use the Hemo-Force Lite where increased venous or lymphatic return is not desired. The Hemo-Force Lite Intermittent Compression System could be contraindicated and should not be used by persons with known or suspected deep vein thrombosis, pulmonary oedema, congestive heart failure, severe arteriosclerosis, thrombophlebitis, or active infection. Do not use on persons with painful and sensitive extremities, where the sleeve will interfere with gangrenous limbs, on persons with vein ligation or recent skin grafts, or extreme deformity of the leg.
NOTE: If you are unsure of any contraindications please refer to the patient’s physician before using the Hemo-Force Lite Intermittent Pneumatic Compression System.

GENERAL SAFETY

These usage and safety guidelines are IMPORTANT! Please follow them carefully.
General Use

1. Carefully unpack the contents of the pump package.
2. Connect the master control unit to a proper power source.
3. Storage Environment Specification.
4. Plug in the unit and verify airflow from the hose connection ports.
5. Place in a dry storage area when not in use.

Storage Environment Specification
It is recommended that the following guidelines be used whenever the system is being stored or transported to another location:

• Temperature limitations: 41°F ~ 140°F (5°C ~ 60°C)
• Relative humidity: 30% ~ 75%

Pump

1. Check the power cord and plug for abrasions and excessive wear.
2. Plug in the unit and verify airflow from the hose connection ports.
3. Place in a dry storage area when not in use.

CONTROL PANEL FEATURES

CONNECTION INSTRUCTION

Step 1 – Connect the air hoses to Control Unit.

Step 2 – Connect the air hoses to sleeves.

PACKING LIST

Package 1 of 1 contains:
1 – Hemo-Force®Lite Pump
1 – Air Tube Pair
1 – User Manual

OPERATING INSTRUCTIONS

The Hemo-Force Lite is easy to set up. The following steps should be followed.
Please read this instruction manual in its entirety before setting up.

1. Once the pump and sleeves have been removed from their packaging plug the pump into an electrical outlet. DO NOT TURN ON YET.

2. Position the pump on any flat surface or suspend the pump at the foot of the bed using the swing-out hooks. Do not hook on a slanted or curved surface.

3. Measure patient’s calf/foot/thigh circumference at the widest point to ensure proper fit.

4. Application of the Calf/Thigh sleeve(s).
   a) Sleeves come in identical pairs and may be used on either leg.
   b) Unfold the sleeve and lay the unfolded sleeve on a flat surface with the inside of the sleeve facing up.
   c) When using dual sleeves, the identical sleeves type (same model) must be used on both legs. Sleeves combinations are calf and calf, thigh and thigh or foot and foot.
   d) Position the sleeves at the appropriate ankle or knee landmark.
   e) Place the patient’s leg on the sleeve lining, position the back of the knee over the popliteal opening in the case of thigh high sleeve.
   f) Starting at the side opposite the air hose, wrap the main flap of the sleeve snugly around the patient’s leg.
   g) Fasten the sleeve securely with the hook and loop fasteners starting at the ankle and then moving to the calf and/or thigh. Secure with tabs starting at the bottom tab marked 1, moving upwards to tab 2 then 3, etc.. Check that none of the hook and loop flaps hang off the end of the sleeve (entirety of hook and loop area is secured to the sleeve). The sleeves should fit securely but not tightly around all parts of the patient’s leg. Confirm sleeve is properly sized by checking that the index line falls between the range markers. Follow the instructions and select the next size up or down if the index line falls out of range.
   h) Use the “two-finger” rule to check that the correct fit is used. Insert 2 fingers horizontally (with palm up and both fingers touching the patient’s leg) in between the sleeve and the patient. This practice should be done at both the top and bottom of the sleeves.
   i) Using the same procedures apply the second identical model sleeve if needed. If only one is to be used, simply leave the unused air outlet on the pump free (no air hose attached).

5. Application of the Foot sleeve(s).
   a) Foot sleeves come in identical pairs and may be used on either foot.
   b) When using dual sleeves the identical sleeves type (same model) must be used on both legs. Do not use in any other combination. Place the sleeve on patient’s foot ensuring the hook and loop attachments are visible.
   c) Ensure a snug fit by placing two fingers around the back of the sleeve to ensure the sleeve is not too tight. Routinely inspect the patient’s feet once compression commences.
   d) Using the same procedures, apply the second identical model sleeve if needed. If only one sleeve is to be used simply leave the unused air outlet on the pump free (no air hose attached).

6. Air hose(s) are required to connect the sleeve(s) to the pump and are provided separately. Attach the sleeve(s) to the air hose(s) using the connectors. Each tube has a male end connector at one end and a female connector at the other. The female end will fit to the male end on the sleeve. Make certain that a click sound is heard to ensure a proper connection.

7. Attach the other end(s) of the air hose(s) (male end) to the female connector(s) on the pump. Make certain that a click is heard with each snap lock connection. If you need to disconnect tubing, firmly pull the male and female connector apart.

8. Press and hold the power button to turn pump on when air hose(s) and sleeve(s) are properly connected.

9. Pump will start initialization process lasting approximately 40 seconds.

10.  The pump will automatically detect single/dual identical model of sleeve(s) during initialization process and will automatically default to the calf/thigh pressure setting.

11. The pump can be manually switched to foot therapy by pressing “FOOT” indicator for 5 seconds while pump is in initialization step. The LED light of “FOOT” will be on when foot therapy is activated.

12. To turn pump off, hold POWER button for 5 seconds.

13. To disconnect device, remove plug from electrical outlet.

14. Respond to the instrument alarms appropriately and refer to troubleshooting guide on pump.

15. To remove the sleeves, firmly pull the connectors apart.

Recommendations during operation

• Avoid placing the tubing and/or any connections or components under the patient as this may negatively impact the effectiveness of the pump and/or cause a skin integrity issue for the patient.
• Make sure that there are no kinks in the tubing and that the connectors are properly locked.
• Never apply or remove the sleeves while inflated as this may cause damage to the sleeve.
• The parts and/or accessories supplied are specifically designed for use with Hemo-Force Lite control unit. Use of other products in conjunction with the system is not recommended.
• Respond to the instrument audio indicator appropriately and follow the manufacturer’s recommendations.

OPERATING FUNCTIONS

1. LOW PRESSURE ALARM:
   a) This device has both a visual and audible low pressure alarm built in. The device constantly monitors the internal pressures of the sleeves to avoid a pressure malfunction from occurring.
   b) If a low pressure is detected, the pump will send a visual and audio alarm warning after two cycles.
   c) Use troubleshooting guide to fix the low-pressure alarm.

2. INDICATOR LIGHT:
   a) Green on Power button: Illuminated to indicate power on with AC power.
   b) Amber: Flashing to indicate a fault has been detected follow by an audio alarm.

CLEANING & DISINFECTION

CAUTION

• Do not use phenol based cleaning solutions.
• Switch off the electrical supply to the pump and disconnect the power cord from the main supply before cleaning and inspection.

The pump: The casing of the pump is manufactured from ABS plastic. If soiled it can be wiped down with a sodium hypochlorite solution to dilution of 1000ppm or any
EPA approved, hospital grade cleaner.
The Sleeve: It is a single patient use sleeve. Do not wash or clean, discard after use.
The control unit(face) should also be cleaned weekly using a damp soft cloth and mild detergent. (Switch off the electrical supply to the pump and disconnect the power cord from the main supply before cleaning and inspection).

ERROR TROUBLESHOOTING GUIDE

Indicates the error information for Hemo-Force Lite, these include:

120mmHg after
2 consecutive cycles.
•  Air hose disconnected at sleeves.| • Check Sleeves application to ensure proper fit.
•  Check for leaks in the sleeves or air hose set and replace if faulty.
•  Turn the pump off and restart.
•  Refer to a service professional if problem persists.
Sleeve Error| •  No sleeves attached during start up.
•  Sleeves are not fully deflated during each restart.
•  The initialization failed due to a possible blockage in air hose/ connectors.| •  Attach sleeves to pump and restart.
•  Ensure sleeves are fully deflated before restart.
•  Check connectors for any blockage and restart.
•  Check air hose connection.
•  Refer to a service professional if problem persists.
HI Pressure/ System Failure| •  Air hose is kinked.
•  Air hose is disconnected at air outlet of the pump.
•  Pressure is greater than set pressure after two consecutive inflations.
•  Pressure is lower than set pressure after 10 consecutive inflations.
•  Electrical malfunction.| •  Check air hose set for any kinks.
•  Attach sleeves to pump and restart.
•  Turn the pump off and restart.
•  Refer to a professional for service if problem persists.

WASTE DISPOSAL

This Product has been supplied from an environmentally aware manufacturer that complies with the WEEE.
This product may contain substances that could be harmful to the environment if disposed of in places (landfills) that are not appropriate according the legislation. Please be environmentally responsible and recycle this product through your recycling facility at its end of life.
INGRESS OF WATER PROTECTION: IP21
The IP Code (or International Protection Rating, sometimes also interpreted as Ingress Protection Rating*) consists of the letters IP followed by two digits and an
optional letter.

• First Digit: Solids
  The first digit indicates the level of protection that the enclosure provides against access to hazardous parts (e.g., electrical conductors, moving parts) and the ingress
  of solid foreign objects.

• Second Digit: Liquids
  Protection of the equipment inside the enclosure against harmful ingress of water.

Against water: Vertical water drips.

TECHNICAL DATA

The Control Unit

Model No.| MDS600INTHL
Size| 9.83” x 4.37” x 8.28”
Weight| 5.29 lbs (2.4 Kg)
Pressure Range| Calf/Thigh Sleeve: 40 mmHg +10/- 5mmHg Foot Sleeve: 120 mmHg + 10/- 5mmHg
Input Rating| AC 100-240V, 50/60Hz, 0.4-0.2A max
Fuse Rating| T2AL 250V
Classification| Class II, Type BF Not AP or APG type
Ingress Protection| IP21
Power Cable| 15ft, non-shielding, AC powered
Operation Humidity| 30-75%
Operation Temperature| 15 – 40°C
Operation Atmospheric Pressure Range| 700 hPa to 1060 hPa
Mode of Operation| Continuous
Applied Part| Sleeve and Air Tube
Sleeves for Hemo-Force® Pump

Model name| Size
MDS601P| Intermittent Sleeve Knee-High Small, Up to 12”, 1pr/Ea
MDS601M| Intermittent Sleeve Knee-High Medium, 12” to 18”, 1pr/Ea
MDS601L| Intermittent Sleeve Knee-High Large, 18” to 22”, 1pr/Ea
MDS601B| Intermittent Sleeve Knee-High X-Large, 22” to 32”, 1pr/Ea
MDS630M| Intermittent Sleeve Thigh-High Medium, 22” to 29”, 1pr/Ea
MDS630L| Intermittent Sleeve Thigh-High Large, 29” to 36”, 1pr/Ea
MDS630B| Intermittent Sleeve Thigh-High X-Large, 36” to 42”, 1pr/Ea
MDS620| Intermittent Foot Medium, Up to 13”, 1pr/Ea
MDS620L| Intermittent Foot Large, 13”-16”, 1pr/Ea
Tubing for Hemo-Force® Pump

Model name| Size
MDS610S| Intermittent Tubing 5 Foot (1.5 Meters)
MDS610L| Intermittent Tubing 10 Foot (3 Meters)

SYMBOLS USED

| ** Type BF Protection Against Electronic Shock| | ** Class II Equipment
---|---|---|---
| Refer to instruction manual| | Waste Disposal
| SGS Certified| | Alternating Current
| Batch Code Ex. 864YYMMXXXX| | Serial Number
| Date of Manufacture| | Catalogue number

ELECTROMAGNETIC COMPATIBILITY

Electric devices may interact due to electro-magnetic radiation. We recommend a safety distance of at least 3.3 feet (1 meter) especially for sensitive equipment.
Upon request, we will provide you with a table for more detailed information.

Recommended separation distances between portable and mobile RF communications equipment and the Hemo-Force Lite

The Hemo-Force Lite is intended for use in an electromagnetic environment (for home healthcare) in which radiated RF disturbances are controlled. The customer or the user of the Hemo-Force Lite

can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Hemo-Force Lite as recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of transmitter
W| Separation distance according to frequency of transmitter m
150 kHz to 80 MHz
d = 1,2| 80 MHz to 800 MHz
d = 1,2| 800 MHz to 2,7 GHz
d = 2,3
0,01| 0,12| 0,12| 0,23
0,1| 0,38| 0,38| 0,73
1| 1,2| 1,2| 2,3
10| 3,8| 3,8| 7,3
100| 12| 12| 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance (d) in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 : At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 : These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.
Guidance and manufacturer’s declaration – electromagnetic emissions

The Hemo-Force Lite is intended for use in the electromagnetic environment (for home healthcare) specified below. The customer or the user of the Hemo- Force Lite should assure that it is used in such an environment.
Emissions test| Compliance| Electromagnetic environment – guidance (for home healthcare environment)
RF emissions CISPR 11| Group 1| The Hemo-Force Lite uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
RF emissions CISPR 11| Class B| The Hemo-Force Lite is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions IEC 61000-3-2| Class A
Voltage fluctuations/ flicker emissions IEC 61000-3-3| Compliance
Guidance and manufacturer’s declaration – electromagnetic immunity

The Hemo-Force Lite is intended for use in the electromagnetic environment (for home healthcare) specified below. The customer or the user of the Hemo- Force Lite should assure that it is used in such an environment.
Immunity test| IEC 60601 test level| Compliance level| Electromagnetic en- vironment – guidance (for home healthcare environment
Electrostatic discharge(ESD) IEC 61000-4-2| Contact:±8 kV
Air±2 kV, ±4 kV, ±8 kV,
±15 kV| Contact:±8 kV
Air±2 kV, ±4 kV, ±8 kV,
±15 kV| Floors should be wood, concrete, or ceramic tile. If floors are cov- ered with synthetic material, the relative humidity should be at least 30 %.
Electrical fast transient/burst IEC 61000-4-4| ±2 kV for power supply lines
±1 kV for input/output lines| ± 2kV for power supply lines
Not applicable| Mains power qual- ity should be that of a typical home health- care environment.
Surge
IEC 61000-4-5| ±0.5 kV, ± 1kV line(s) to line(s)
±0.5 kV, ± 1kV, ± 2kV
line(s) to earth| ± 0.5 kV, ± 1kV line(s) to line(s)
Not applicable| Mains power qual- ity should be that of a typical home health- care environment.
Voltage Dips, short in- terruptions and voltage variations on power supply input lines IEC 61000-4-11| Voltage dips:
0 % UT; 0,5 cycle
0 % UT; 1 cycle
70 % UT; 25/30 cycles
Voltage interruptions: 0 % UT; 250/300 cycle| Voltage dips:
0 % UT; 0,5 cycle
0 % UT; 1 cycle
70 % UT; 25/30 cycles
Voltage interruptions: 0 % UT; 250/300 cycle| Mains power quality should be that of a typ- ical home healthcare environment. If the user of the Hemo- Force Lite requires continued operation during power main interruptions, it
is recommended that the Hemo-Force Lite be powered from an uninterruptible power supply.
Power frequency(50, 60 Hz) magnetic field IEC 61000-4-8| 30 A/m
50 Hz or 60 Hz| 30 A/m
50 Hz, 60 Hz| The Hemo-Force Lite power frequency mag- netic fields should be at levels characteristic of a typical location in a typical home health- care environment.
NOTE : UT is the a.c. mains voltage prior to application of the test level.
Guidance and manufacturer’s declaration – electromagnetic immunity (cont)

The Hemo-Force Lite is intended for use in the electromagnetic environment (for home healthcare) specified below. The customer or the user of the Hemo- Force Lite should assure that it is used in such an environment.
Immunity test| IEC 60601 test level| Compliance level| Electromagnetic environment – guidance (for home healthcare environment)
Conducted RF IEC 61000-4-6
Radiated RF IEC 61000-4-3| 3 Vrms:
0,15 MHz – 80 MHz
6 Vrms:
in ISM and amateur radio bands between 0,15 MHzand 80 MHz
80 % AM at 1 kHz
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz| 3 Vrms:
0,15 MHz – 80 MHz
6 Vrms:
in ISM and amateur radio bands between 0,15 MHz
and 80 MHz
80 % AM at 1 kHz
10 V/m
80 MHz – 2,7 GHz
80 % AM at 1 kHz| Portable and mobile RF communica- tions equipment should be used no closer to any part of the Hemo-Force Lite , including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.
Recommended separation distance
d = 1,2
d = 1,2 80 MHz to 800 MHz
d = 2,3 800 MHz to 2,7 GHz
Where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommend- ed separation distance in metres (m).
Interference may occur in the vicinity of equipment marked with the following symbol:
NOTE 1 : At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2 : These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
Guidance and manufacturer’s declaration – electromagnetic immunity Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communications equipment

The Hemo-Force Lite is intended for use in the electromagnetic environment (for home healthcare) specified below. The customer or the user of the Hemo- Force Lite should assure that it is used in such an environment.
Test frequency (MHz)| Band a) (MHz)| Service a)| Modulation b)| Maximum power (W)| Distance (m)| IMMUNITY TEST LEVEL (V/m)| Compliance LEVEL (V/m)
(for home health- care)
385| 380- 390| TETRA 400| Pulse modulation b) 18 Hz|

1,8

| 0,3| 27| 27
450| 430- 470| GMRS 460, FRS 460| FM c) ±5 kHz deviation
1 kHz sine| 2| 0,3| 28| 28
710| 704- 787| LTE Band 13, 17| Pulse modulation b) 217 Hz| 0,2| 0,3| 9| 9
745
780
810| 800- 960| GSM 800/900, TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5| Pulse modulation b) 18 Hz| 2| 0,3| 28| 28
870
930
1720| 1700- 1990| GSM 1800;
CDMA 1900;
GSM 1900; DECT;
LTE Band 1, 3,
4, 25; UMTS| Pulse modulation b) 217 Hz| 2| 0,3| 28| 28
1845
1970
2450| 2400- 2570| Bluetooth, WLAN, 802.11b/g/n, RFID 2450,

LTE Band 7

|

Pulse modulation b) 217 Hz

| 2| 0,3| 28| 28
5240| 5100- 5800| WLAN 802.11a/n| Pulse modulation b) 217 Hz| 0,2| 0,3| 9| 9
5500
5785
NOTE : If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting antenna and the ME EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m test distance is permitted by IEC 61000-4-3.

Guidance and manufacturer’s declaration – electromagnetic immunity Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communications equipment (cont)
The Hemo-Force Lite is intended for use in the electromagnetic environment (for home healthcare) specified below. The customer or the user of the Hemo- Force Lite should assure that it is used in such an environment.
a) For some services, only the uplink frequencies are included.
b) The carrier shall be modulated using a 50 % duty cycle square wave signal.
c) As an alternative to FM modulation, 50 % pulse modulation at 18 Hz may be used because while it does not represent actual modulation, it would be worst case.
CAUTION: If abnormal behavior is observed due to EM disturbances, please relocate the device accordingly.
CAUTION: Please do not use any other cables or accessories not approved by the manufacturer in this manual to avoid negative influence on electromagnetic compatibility.

EXPECTED SERVICE LIFE

To maintain basic safety and essential performance in regards to EMC, the HemoForce Lite pump has an expected service life of two years. To maintain the condition of the pump have the pump serviced regularly according to the schedule recommended by Medline Industries, Inc. DO NOT use unapproved accessories or attempt to modify, disassemble or otherwise misuse the Hemo- Force Lite system or any of its components.
Medical electrical equipment needs special precautions regarding EMC. Shall the device be used within one mile distance from AM, FM, or TV broadcast antennas, it needs to be installed according to the EMC information provided.

WARRANTY

Medline Industries, Inc. guarantees that this equipment is free from defects in materials and workmanship. Our obligation under this warranty is limited to the repair of equipment returned to the place of purchase within two years of the delivery date.
We agree to service / adjust any equipment returned, and to replace or repair any part that is proven to be a warranty defect, at no charge within the warranty time period.
This warranty excludes equipment damage through shipping, tampering, improper maintenance, carelessness, accident, negligence or misuse, or products that have been altered, repaired or dismantled other than with the manufacture’s written authorization and by its approved procedures and by properly qualified technicians.
In no event shall Medline products be liable for any direct, indirect or consequential damages or losses resulting from the use of equipment.

Medline Industries, LP. Three Lakes Drive, Northfield, IL 60093
Medline United States
1-800-MEDLINE (633-5463)
medline.com
info@medline.com
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