EGA-500P Irrigation Pump Instructions for Use Rev M

CONTENT

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Table Of Contents I.

Unpacking And Inspection:...3

II.

Introduction:...3 Definitions:...3 Indications For Use:...3 Contra-indications:...3

III. Warnings And Cautions...4 IV. Product Features...6 Theory Of Operation...6 V.

Technical Specifications...6 Electrical Specifications...6 Mechanical Specifications...7 Flow Rates...7 Environmental requirements...7 Accessory Items...8

VI. Front Panel Controls/Connections...9 VII. Rear Panel Connections...10 VIII. Setup And Operation...11 Initial Setup...11 Pre-Procedure setup...12 Water Pre-Warming...13 Operation...13 Shutdown...13 IX. Care and Maintenance...14 Cleaning...14 Maintenance...14 X.

Electromagnetic Compatibility (EMC) Information...15

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Instruction Manual I. Unpacking And Inspection: Upon receiving the PENTAX® Medical IRRIGATION PUMP, ensure that the following items are contained in the shipping box: • Base tray and water bottle holder • Hardware to assemble base tray and water bottle holder • Operator’s manual • Power cord • Foot pedal • Pump Head

READ THIS MANUAL THOROUGHLY BEFORE PROCEEDING WITH THE OPERATION OF THIS EQUIPMENT. These instructions should be stored and used for reference as needed. If there are any questions, please contact your local PENTAX service facility.

II. Introduction: Definitions: • Throughout this document the PENTAX Medical IRRIGATION PUMP may be referred to as “unit” or “device” • mL/min – milliliters per minute (flow) • VAC – Volts Alternating Current (electrical potential) • kPa – kilo Pascal (pressure) • W – Watts • VA – Volt Amps • Hz – Hertz (frequency)

Indications For Use: Federal (USA) law restricts this device to sale by or on the order of physician. The PENTAX Medical IRRIGATION PUMP is indicated for GI endoscopic irrigation with room temperature or warm water for use with washing catheters, integral GI endoscope water jet channels and GI endoscope working channels.

The device contains a heated water bottle cradle that is intended to maintain a sterile water bottle for GI endoscopic irrigation at a maximum temperature set point of 37°C with a tolerance of ± 3°C.

Contra-indications: The device should only be used for GI endoscopic procedures requiring irrigation of the gastrointestinal tract and should not be used for any other treatments or procedures. The device is not intended for use with or exposure to magnetic resonance imaging (MRI) systems. Do not use the device in an environment where it could be exposed to MRI systems.

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III. Warnings And Cautions SIGNAL WORDS: WARNING: Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.

CAUTION: Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury. It may also be used to alert against unsafe practices or potential equipment damage.

Safety Symbols:

Attention

Refer To Operating Instructions

Warning: Dangerous Voltage

Equipotentiality

DO NOT Allow Fingers To Contact Moving Parts.

Hot Surface

MR Unsafe

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WARNINGS A. To reduce risk of electrical shock, do not remove cover. Refer servicing to qualified service personnel. B. To avoid the risk of electric shock, this equipment must only be connected to a supply mains with protective earth ground. C. The PENTAX® Medical IRRIGATION PUMP is not suitable for use in the presence of a flammable anesthetic mixture with oxygen. D. The PENTAX Medical IRRIGATION PUMP shall be sold only by prescription for use by physicians/clinicians who are trained regarding the amount of water to use for irrigation and infusion. E. Always watch for abnormal flow rates and adjust the flow rate as necessary. If an unusual flow rate remains after adjustments have been made, then stop the procedure and investigate. F. Only qualified medical personnel in an acceptable medical facility should operate the PENTAX Medical IRRIGATION PUMP. G. The PENTAX Medical IRRIGATION PUMP should be connected to a properly grounded 120V receptacle marked “Hospital Grade” or “Hospital Only,” otherwise grounding reliability cannot be achieved. H. Extreme precaution must be taken when handling liquids around electrical equipment. DO NOT operate the PENTAX Medical IRRIGATION PUMP if liquid has been spilled on the unit. I. The PENTAX Medical IRRIGATION PUMP should not be used adjacent to or stacked with other equipment other than another PENTAX Medical device. Electromagnetic or other interference may occur between the PENTAX Medical IRRIGATION PUMP and other electronic devices. If stacked or adjacent use is necessary, the equipment or system should be observed to verify normal operation in the configuration in which it will be used. J. The PENTAX Medical IRRIGATION PUMP should only be used in conjunction with other equipment whose safety against leakage currents has been established. K. The instructions contained in the operating manuals of any equipment to be used in conjunction with the PENTAX Medical IRRIGATION PUMP must be followed to avoid any possible hazard from incompatibility. L. The instructions for use described in this manual MUST be followed. Otherwise, compromised safety, malfunction, injury to the operator and/or patient, or costly damage to the unit and other equipment may occur. M. The PENTAX Medical IRRIGATION PUMP must be connected to an appropriate power source when loss of power source would result in an unacceptable risk.

CAUTION A.

If emergency or abnormal function occurs, immediately turn off the power to the unit.

B.

Field-servicing of the PENTAX Medical IRRIGATION PUMP is limited to the replacement of the power cords, water bottle holder and heater assemblies, pump heads, foot pedals and fuses.

C.

Remove power from the device before initiating any field servicing of the replacement parts.

D.

There are no user serviceable parts inside the PENTAX Medical IRRIGATION PUMP unit. Repairs to the PENTAX Medical IRRIGATION PUMP should only be performed by qualified service personnel.

E.

Do not use the device if the enclosure is damaged or enclosure integrity has been compromised.

F.

Do not attempt to operate the device before reading and understanding all sections of this manual.

G.

Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in Section X.

H.

Portable and mobile radio frequency (RF) communications equipment can affect medical electrical equipment. Do not expose the device to sources of electromagnetic interference such as CT equipment, diathermy equipment, cellular phones, RFID tags and metal detectors.

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IV. Product Features • • • • • •

Built in water bottle warmer maintains water at up to 37°C with an allowable tolerance of ± 3°C “Prime” feature runs pump for 20 seconds with automatic timer Includes side water bottle clip for traditional water bottle holder Safety feature prevents pump from running when pump head is open Robust motor design for consistent performance Water bottle holder is angled for easier access to water bottle and tubing

Theory Of Operation The PENTAX® Medical IRRIGATION PUMP works by turning a peristaltic-roller-type pump head to move liquid through a tube set and into a GI endoscope system. The pump head will not operate if the pump head is open, and will cease to operate if the pump head is opened while the motor is activated. The unit incorporates a “prime” feature which allows the unit to operate for a pre-set period of time. This feature can be canceled while in progress by pressing the foot pedal. The water bottle warmer is intended to maintain the warmth of the water in a sterile water bottle that has been pre-warmed. It is controlled by dual temperature sensors for redundancy and safety. There is a heating element integrated into the water bottle holder which then radiates heat through the bottle and into the water. The temperature of the water bottle holder is maintained at a maximum of 37°C ± 3°C.

V. Technical Specifications Electrical Specifications Input Voltage:

100-240 VAC

Input Frequency:

50-60 Hz

Power Consumption:

110 VA

Fuse Rating:

M10AL250V Medium acting, 10 amp, low breaking capacity, 250 volt Replace fuses only with those of same type and rating

Certifications:

IEC-60601-1, IEC-60601-1-2, IEC-60601-2-18

Classification:

Class 1 Type B

Water Bottle Warmer:

20W resistive element with dual temperature sensors.

IP Rating (Ingress Protection):

IP24

WARNING: Grounding reliability can only be achieved when connected to a receptacle marked “Hospital Grade”.

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Mechanical Specifications Physical Dimensions: Height

4 ¾” inches

121 mm

Width

7 ¾” inches

197 mm

Depth

13 ¾” inches

349 mm

Weight

10.5 pounds

4.8 kg

Flow Rates Auxiliary Water Channel

0-300 ml/min*

Biopsy Channel

0-650 ml/min*

*These values are approximate and are based on an average flow obtained with three different manufacturer’s GI endoscopes with biopsy channel diameters ranging from 2.8 mm - 4.2 mm and auxiliary water channel diameters ranging from 0.8mm - 0.1 mm. User results may vary depending on scope used, channel size and working channel length.

CAUTION: The PENTAX® Medical IRRIGATION PUMP is intended for use only by physicians/ clinicians who are trained regarding the amount of water to use for irrigation and infusion during GI endoscopic procedures. Environmental requirements Operating Temperature:

16° to 24°C (+61° to 75°F)

Operating Relative Humidity:

30% to 75% non-condensing

Operating Pressure:

70 kPa-106 kPa_(10.2 PSI -15.4 PSI)

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Accessory Items The PENTAX® Medical IRRIGATION PUMP, EGA‑500P, is intended to be used only with the specific models of compatible tubing sets, connectors and accessories identified in the table below and/or officially recommended by PENTAX. Use of the device with accessories not identified in the table below or officially recommended by PENTAX may result in incompatibility and/or the risk of cross-contamination and infection transmission.

Order Number

Description

100150CO2P, 100150CO2UP (24 hr Use)

PENTAX Medical DispoCap CO2

100160P, 100160UP (24 hr Use)

PENTAX Medical DispoCap Air

100130P, 100130UP (24 hr Use)

PENTAX Medical Irrigation Tubing For EGA‑500P

200230P, 200230UP (24 hr Use)

PENTAX Medical Irrigation Tubing For EGP-100P

100242P (Single use only)

PENTAX Medical Single Use Waterjet Connector

100116P (24 hr Use)

PENTAX Medical 24 hr Use Waterjet Connector

100551P

PENTAX Medical CO2 Source Tubing

Replacement Parts EGA‑500P Item

Order Number

Power cord

EGA‑7014

Water Bottle holder And Warmer Assembly

EGA‑7010

Pump Head

EGA‑7016

Foot Pedal

47049-942

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VI. Front Panel Controls/Connections NOTE: All status indicator lights will be green during normal operation. 1.

On/Off Push Button Turns main power on or off to the unit

2.

Water Bottle Warmer On/Off Push to turn water warmer on or off

3.

Pump Flow Control The flow control knob is a continuous variable flow control that has settings between 0 and 100% flow. The lowest knob setting corresponds to no flow while the max flow control setting represents 100% flow. It contains bracketed visual iterations to represent flow magnitude in increasing increments of approximately 10%, however the flow control knob response is not entirely linear. Incremental flow control knob increases between 50-100% have a larger impact on flow rate response as compared to incremental changes between 0-50%.

Flow Rates: Auxiliary Water Channel

0-300 ml/min*

Biopsy Channel

0-650 ml/min*

*These values are approximate and are based on an average flow obtained with three different manufacturer’s GI endoscopes with biopsy channel diameters ranging from 2.8 mm-4.2 mm and auxiliary water channel diameters ranging from 0.8 mm-1.0mm. User results may vary depending on scope used, channel size and working channel length.

CAUTION: The PENTAX® Medical IRRIGATION PUMP is intended for use only by physicians/ clinicians who are trained regarding the amount of water to use for irrigation and infusion during GI endoscopic procedures. 4.

Foot Pedal Connection

5.

Prime Button When pressed, pump will run for a period of 20 seconds. The cycle can be canceled at any time by either pressing the foot pedal or prime button again. See Section VIII for full explanation.

6.

Pump Head Refer to Section VIII for assembly instructions

2

1

3

4

5

6

(The appearance of your device may differ slightly from picture shown above)

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VII. Rear Panel Connections 1.

Water Bottle Warmer Connection Power connection for water bottle warmer

2.

Equipotentiality (Earth Ground)

3.

AC Power Connection AC power input 100-240 VAC, 50-60HZ

WARNING: Use only the hospital grade power line cord supplied with this unit. Connect only to a power receptacle marked as hospital grade. 4.

Fuse Receptacle

WARNING: Replace only with type and rating marked M10AL250V 5.

Water Bottle Holder And Warmer The water bottle holder contains the heating element and an integral hold-down bracket to secure the water bottle in place.

5

1

2

3

(The appearance of your device may differ slightly from picture shown above)

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4

VIII. Setup And Operation Initial Setup 1.

Before beginning, inspect the PENTAX® Medical IRRIGATION PUMP for any signs of damage.

2.

Install the pump head onto the device by aligning the flat shaft on the front of the device with the slotted hole in the pump head and rotate the pump head until it locks in place.

3.

Assemble the water bottle holder and warmer assembly in the following manner: A. The following supplies are necessary and can be found in a bag attached to the water bottle holder: a.)

Short Screws (2)

b.)

Long Screws (2)

c.)

Large Hex Key

d.)

Small Hex Key

B. Attach the water bottle holder to the base tray using the (2) small screws and small hex key.

C. Place the PENTAX Medical IRRIGATION PUMP on the base tray and install the (2) long screws using the arge hex key.

D. Adjust the water bottle hold-down bracket to fit the water bottles used by your facility. This is done by loosening the nut on the back and sliding the bracket up or down so it contacts the water bottle and then re-tightening the nut.

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4. 5. 6. 7.

Plug the water warmer cable into the receptacle marked “water warmer” on the back of the unit. Place the PENTAX® Medical IRRIGATION PUMP on a flat surface such as an endoscope accessory cart or other suitable working surface. Before connecting the power cord to the hospital grade wall receptacle, make sure the power is off to the device, and no accessories are connected. Connect the power cord to the back of the device.

Pre-Procedure setup 1. 2.

Place the foot pedal on the floor and insert the foot pedal cord into the designated front panel receptacle. Insert a water bottle containing sterile water into the water bottle holder

CAUTION: Use of irrigation fluid other than sterile water can pose an infection risk to patients. Adjust the hold-down bracket by loosening the knob, lowering the bracket until it contacts the top of the bottleand then tightening the adjusting screw. After initial setup, if the same size and type of bottle is used, it should require no further adjustment. 3.

Open a sterile pouch of the 100130P PENTAX Medical irrigation tubing. Read and follow its instructions for use.

CAUTION: The PENTAX Medical IRRIGATION PUMP EGA‑500P is intended to be used only with specific models of compatible tubing sets, connectors and accessories identified in the table in Section V or officially recommended by PENTAX. Use of the device with accessories not identified in the accessories table or officially recommended by PENTAX may result in incompatibility and/or the risk of cross contamination and infection transmission. 4.

Connect the tubing to the water bottle.

5.

Open the pump head and place the tubing into the pump head rollers so that the water flow will be from right to left facing the pump.

Note: The device is equipped with a safety feature so that the pump will not operate if the pump head is open. 6. 7.

Turn the flow rate indicator to its lowest speed and turn the unit on. Perform the following procedure to ensure the tubing is fully filled with sterile water each time before connecting to a GI endoscope: A. Direct the end of the tube into a receptacle capable of catching expelled water. B. Depress the foot switch and turn up the flow rate adjustment to the desired level based on the irrigation connection to the GI endoscope.

PRIME FUNCTION: The prime function allows the user to perform this feature with the assistance of an automatic timer in lieu of pressing the foot pedal. Pressing the prime button will run the pump for a period of 20 seconds. If at any time the prime cycle needs to be stopped the button can be pressed again, or the foot pedal can be pressed. The prime function is not intended to be a definite means of fully priming the tubing. It is the responsibility of the end user to ensure the tubing and GI endoscope channel are fully filled with water before proceeding. 8.

When priming is complete, attach the irrigation tube set to the GI endoscope using the proper adapter for the endoscope model and endoscope channel. (See Section V for a complete list of irrigation tubing and adaptors for various GI endoscopes.)

9.

The PENTAX Medical IRRIGATION PUMP is now ready to use.

CAUTION: NEVER allow the sterile water bottle to empty completely to avoid air entering the irrigation tubing.

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Water Pre-Warming 1.

The PENTAX® Medical irrigation pump has an integral water warming system that can maintain the temperature of the water at up to 37 ± 3°C.

NOTE: The system is not intended to raise the temperature of the water; therefore pre-warming of the water bottle is required. 2.

Place sterile water bottle in a fluid warming oven set to 37°C for at least 2 hours until the water has been warmed to at least 37 ± 3°C. Do not exceed this temperature. If warm water is not desired, turn the water warmer on the pump off and place a bottle of room temperature sterile water on the water bottle holder.

NOTE: If the water warmer has been enabled and has exceeded the upper temperature set point limit, the water warmer’s switch indicator light will turn blue and the warmer will automatically shut off. If the switch indicator light is flashing blue, ensure the water warmer cable is plugged into the back of the unit. If it is connected and the light is flashing, this may indicate a problem with the unit. Contact customer service at 800-444-4729. Read and become familiar with all manufacturer’s instructions on warming ovens and water bottles regarding maximum fluid temperatures. Never exceed 40°C during water pre-warming.

CAUTION: Never use a microwave oven to warm a water bottle as this could heat the water to a dangerously high temperature or could result in uneven warming.

CAUTION: The surface of the water bottle warmer may be hot to the touch.

Operation 1.

Water flow is initiated by pressing the foot pedal and releasing when no longer desired.

2.

If more water flow is required, increase the flow control setting on the front panel. Refer to Section VI for flow rates.

Note: The device is equipped with a safety feature so that the pump will not operate if the pump head is open. The physician must assess the condition of the patient and use clinical judgment to set the flow rate from the pump to a suitable level to avoid patient trauma. The flow control should always be set at the lowest setting at the start of the procedure and be increased incrementally to a level commensurate with the clinical condition of the patient and the degree of irrigation required.

Shutdown 1.

Press the power button to turn the unit off. The light should extinguish.

2.

If the warming element has been activated, press the power button for the warmer to turn off. The blue light should extinguish.

3.

After the procedures are complete for the day, remove the tubing from the pump head and discard the tubing and water bottle.

Note: ENDOGATOR™ Irrigation tubing may be used for 24 hours.

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IX. Care and Maintenance Cleaning •

Before cleaning ensure the power to the unit is turned off and the electrical cord unplugged.

•

The outside surface of the PENTAX® Medical IRRIGATION PUMP can be cleaned with a damp cloth, 70% isopropyl alcohol solution, or a 10% bleach with water solution as often as deemed necessary.

•

Do not use abrasive or harsh cleaners.

•

Do not allow liquid to enter the unit.

•

To disinfect the outside surface, use a mild disinfectant according to the manufacturer’s instructions.

•

Do not sterilize the unit by any means.

Maintenance Pump Head Maintenance If liquids are spilled onto the pump head, it should be removed and cleaned with a mild detergent. Remove any tubing from the pump head prior to removal for cleaning. The same cleaning procedure should be used to limit the build-up of dust (which can become electrostatically charged and/or heated by friction).

Servicing The unit is not user serviceable. Please contact your local PENTAX service facility.

Limited Warranty Materials and workmanship of this product, PENTAX Medical IRRIGATION PUMP will be warranted for a period of one (1) year from the original date of purchase. If this product should become inoperable due to a defect in materials or workmanship during this one (1) year warranty period, the product will be repaired or replaced. This limited warranty does NOT include replacement or service due to an accident, natural disaster, use of the product other than specified, external electrical error, improper installation, negligence, modification, unauthorized service or normal wear. Disposal No special care is needed when disposing of the device.

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X. Electromagnetic Compatibility (EMC) Information Medical electrical equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in this section. Portable and mobile RF communications equipment can affect medical electrical equipment. Do not expose the device to sources of electromagnetic interference such as CT equipment, diathermy equipment cellular phones, RFID tags and metal detectors. The use of accessories, transducers and/or cables other than those specified, with the exception of those sold by the manufacturer as replacement parts for internal components, may result in increased emissions or decreased immunity of the equipment or system. The equipment or system should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is neccessary, the equipment or system should be observed to verify normal operation in the configuration in which it will be used.

Table 1 – Guidance And MANUFACTURER’S Declaration ELECTROMAGNETIC EMISSIONS For All ME EQUIPMENT And ME SYSTEMS Guidance and Manufacturer’s Declaration – Emissions The EGA‑500P is intended for use in the electromagnetic environment specified below. The customer or user of the EGA‑500P should ensure that it is used in such an environment. Emissions Test

Compliance

RF Emissions CISPR 11

Group 1

RF Emissions CISPR 11

Class A

Harmonics IEC 61000-3-2

Class A

Flicker IEC 61000-3-3

Complies

Electromagnetic EnvironmentGuidance The EGA‑500P 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. The EGA‑500P is suitable for use in all establishments, other than domestic, and those directly connected to the public lowvoltage power supply network that supplies buildings used for domestic purposes.

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Table 2 – Guidance And MANUFACTURER’S Declaration Electromagnetic IMMUNITY For All ME EQUIPMENT And ME SYSTEMS Guidance and Manufacturer’s Declaration – Electromagnetic Immunity The EGA‑500P is intended for use in the electromagnetic environment specified below. The customer or user of the EGA‑500P should ensure that it is used in such an environment. EN/IEC 60601 Test Level

Compliance Level

ESD EN/IEC 61000-4-2

±6kV Contact ±8kV Air

±6kV Contact ±8kV Air

Floors should be wood, concrete or ceramic tile. If floors are synthetic, the r/h should be at least 30%.

EFT EN/IEC 61000-4-4

±2kV Mains ±1kV I/Os

±2kV Mains ±1kV I/Os

Mains power quality should be that of a typical commercial or hospital environment.

Surge EN/IEC 61000-4-5

±1kV Differential ±2kV Common

±1kV Differential ±2kV Common

>95% Dip for 0.5 Cycle

>95% Dip for 0.5 Cycle

60% Dip for 5 Cycles

60% Dip for 5 Cycles

30% Dip for 25 Cycles

30% Dip for 25 Cycles

>95% Dip for 5 Seconds

>95% Dip for 5 Seconds

3A/m

3A/m

Immunity Test

Voltage Dips/Dropout EN/IEC 61000-4-11

Power Frequency 50/60Hz Magnetic Field EN/IEC 61000-4-8

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Electromagnetic Environment – Guidance

Mains power quality should be that of a typical commercial or hospital environment.

Mains power quality should be that of a typical commercial or hospital environment. If the user of the EGA‑500P requires continued operation during power mains interruptions, it is recommended that the EGA‑500P be powered from an uninterruptible power supply or battery. Power frequency magnetic fields should be that of a typical commercial or hospital environment.

Table 3 – Guidance And MANUFACTURER’S Declaration Electromagnetic IMMUNITY For ME EQUIPMENT And ME SYSTEMS That Are Not LIFE-SUPPORTING Guidance and manufacturer’s declaration – Electromagnetic Immunity The EGA‑500P is intended for use in the electromagnetic environment specified below. The customer or user of the EGA‑500P should ensure that it is used in such an environment. Immunity Test

EN/IEC 60601 Test Level

Compliance Level

Electromagnetic Environment – Guidance Portable and mobile communications equipment should be separated from the EGA‑500P by no less than the distances calculated/listed below: D=(3.5/V1)(Sqrt P) D=(3.5/E1)(Sqrt P) 80 to 800 MHz

Conducted RF EN/IEC 61000-4-6

3 Vrms 150 kHz to 80 MHz

(V1)Vrms = 3 Vrms

Radiated RF EN/IEC 61000-4-3

3 V/m 80 MHz to 2.5 GHz

(E1)V/m = 3 V/m

D=(7/E1)(Sqrt P) 800 MHz to 2.5 GHz Where P is the max power in watts and D is the recommended separation distance in meters. Field strengths from fixed transmitters, as determined by an electromagnetic site survey, should be less than the compliance levels (V1 and E1). Interference may occur in the vicinity of equipment containing a transmitter.

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Table 4 – Recommended Separation Distances Between Portable And Mobile RF Communications Equipment And The ME EQUIPMENT Or ME SYSTEM For ME EQUIPMENT And ME SYSTEMS That Are Not LIFE-SUPPORTING Recommended Separations Distances for the EGA‑500P The EGA‑500P is intended for use in the electromagnetic environment in which radiated disturbances are controlled. The customer or user of the EGA‑500P can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment and the EGA‑500P as recommended below, according to the maximum output power of the communications equipment. Max Output Power (Watts)

Separation (m) 150kHz to 80MHz

Separation (m) 80 to 800MHz

Separation (m) 800MHz to 2.5GHz D=(7/E1)(Sqrt P)

D=(3.5/V1)(Sqrt P)

D=(3.5/E1)(Sqrt P)

0.01

.1166

.1166

.2333

0.1

.3689

.3689

.7378

1

1.1666

1.1666

2.3333

10

3.6893

3.6893

7.3786

100

11.6666

11.6666

23.333

Approved accessories 3.7m

Manufacturer/Model

Maximum length

Power cable

Interpower/86610610

3.7m

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Distributed by: PENTAX Medical (Shanghai) Co., Ltd.

Room 701, 291 Fumin Road, Shanghai, China 200031 Tel: +86-21-61701555 Fax: +86-21-61701655

PENTAX Medical Singapore Pte. Ltd.

438A Alexandra Road, #08-06 Alexandra Technopark Singapore 119967 Tel: +65-6271-1669 Fax: +65-6271-1691

PENTAX Medical Company A Division of PENTAX of America, inc.

3 Paragon Drive Montvale, New Jersey 07645-1782 USA Tel: +1-201-571-2300 Toll Free: +1-800-431-5880 Fax: +l-201-391-4189

Manufactured in the USA by: Medivators Inc. 14605 28th Avenue North Minneapolis, MN 55447 USA Toll Free: +1.800.444.4729

www.medivators.com

Medivators BV Sourethweg 11 6422PC Heerlen The Netherlands Tel: +31.45.5.471.471

printed in USA

IFU-66 / REV M