Dulong Medtech SMR MAXI Deluxe User manual

110-014-008 Rev B
ECO 203160 Date E󰀨ective: November 2020
SMR® MAXI® Cabinet
OWNER’S MANUAL
Deluxe, Mini, Standard, and Tall
MAXI Cabinet
TM
I
O

When contacting Dulong Medtech for Customer Service, it will be helpful if
you have your Customer Identication Number and your Customer Order
Number available. Please take a moment to record these numbers (printed on
invoice) in the spaces below.
Customer Identication Number: ___________________________________
Customer Order Number:__________________________________________
5605 ST-FRANCOIS
ST-LAURENT, QUEBEC, H4S 1W6
CANADA
© COPYRIGHT 2020, GLOBAL SURGICAL CORPORATION. NO PART OF THIS PUBLICATION MAY BE
COPIED, PHOTOCOPIED, REPRODUCED, TRANSLATED, OR REDUCED TO ANY ELECTRONIC MEDIUM
OR MACHINE-READABLE FORM, IN WHOLE OR IN PART, WITHOUT THE PRIOR WRITTEN CONSENT
OF GLOBAL SURGICAL CORPORATION, 3610 TREE COURT INDUSTRIAL BLVD., ST. LOUIS, MO 63122
COPYRIGHT NOTICE

Congratulations on your purchase of the
SMR MAXI Cabinet.
We truly appreciate your business,
and we’re grateful for the trust you’ve placed in us.

TABLE OF CONTENTS
Section 1 Important Safety Instructions ........................................................................................ 1-1
1.1. Symbol Denitions .............................................................................................................. 1-1
1.2. Warnings and Cautions ...................................................................................................... 1-2
Section 2 Unpacking Instructions .................................................................................................. 2-1
2.1. Pump Connections .............................................................................................................. 2-2
2.2. Setting Up the S WA77710 Wall Transformer .................................................................... 2-3
2.3. Setting Up the 123-000-072 HEINE NT300 Otoscope Charger......................................... 2-3
Section 3 Product Information ....................................................................................................... 3-1
3.1. Description ........................................................................................................................... 3-1
3.2. System Parts ....................................................................................................................... 3-2
3.3. Specications ...................................................................................................................... 3-3
3.4. Vacuum Pump and Canister System Specications ........................................................ 3-4
3.5. Pressure Pump Specications ........................................................................................... 3-4
3.6. S 7401355 Suction/Pressure Foot Switch (Optional) Specications .............................. 3-4
3.7. Optional Equipment ............................................................................................................ 3-5
Section 4 Operating Instructions ................................................................................................... 4-1
4.1. Operation and Controls ...................................................................................................... 4-1
4.2. Control Panel - Main Power Switch ................................................................................... 4-1
4.3. Control Panel - Vacuum/Pressure Switch ......................................................................... 4-1
4.4. Illumination Controls/ Otoscope Heads ............................................................................ 4-1
4.4.2. Rechargeable Instruments ................................................................................................. 4-2
4.5. Optional Light Source ......................................................................................................... 4-4
4.5.1. Optional S 740200LED LED Light Source With Turret ..................................................... 4-4
4.5.1.1. Powering Up The LED Light Source .................................................................................. 4-4
4.6. Optional S 740258A Drawer Warmer ............................................................................... 4-5
4.6.1. Powering Up the Drawer Warmer ....................................................................................... 4-5
4.7. Optional S 740254KP Keyless Locking System ............................................................... 4-5
4.7.1. How to Operate the S 740254KP Keyless Locking System ............................................. 4-5
4.8. Optional S 7401355 Suction / Pressure Foot Switch........................................................ 4-6
4.9. Pump Controls ..................................................................................................................... 4-6
4.9.1. Vacuum Pump Controls ...................................................................................................... 4-6
4.9.2. Pressure Pump Controls .................................................................................................... 4-6
4.9.3. Pressure Adjustment .......................................................................................................... 4-7
4.10. Attaching Glassware or Suction Instruments ................................................................... 4-7
4.10.1. Atomizer Instruments .......................................................................................................... 4-7
4.10.2. Suction Instruments ............................................................................................................ 4-7

TABLE OF CONTENTS
Section 5 Care and Maintenance ................................................................................................... 5-1
5.1. Cleaning and Disinfecting ................................................................................................... 5-1
5.1.1. Preparation and Best Practice ............................................................................................ 5-1
5.1.2. Disposable Items .................................................................................................................. 5-1
5.1.3. Glassware, Otoscopes, Mirror Warmer and Lightsource ................................................. 5-2
5.1.4. Stainless Steel Surfaces ...................................................................................................... 5-2
5.1.5. Aluminum Composite and Laminate Surfaces .................................................................. 5-2
5.1.6. Wilsonart® Work Surface ................................................................................................. 5-2
5.2. General Maintenance ........................................................................................................... 5-3
5.3. Replacing the S 600001 Disposable Canister .................................................................... 5-4
5.4. Replacing the S 740600C Disposable Canister Liner........................................................ 5-6
5.5. Replacing the S 850020 Hydrophobic Filter....................................................................... 5-7
5.6. Cleaning and Disinfecting the Optional S 740200LED LED Light Source With Turret ... 5-8
5.7. Replacing the fuse in the Optional S 740200LED LED Light Source............................... 5-8
5.7. Replacing the Batteries in the S 740254KP Keyless Locking System .......................... 5-10
5.7.1. Care and Cleaning of the S 740254KP Keyless Locking System ................................... 5-10
5.8. 123-007-072 Otoscope Battery Replacement ................................................................... 5-10
5.9. S 740275 USB Auxiliary Outlet .......................................................................................... 5-11
5.10. Servicing The S 740258A Drawer Warmer ........................................................................ 5-11
Section 6 Troubleshooting .............................................................................................................. 6-1
6.1. Troubleshooting Low Suction ............................................................................................. 6-1
6.2. Troubleshooting the S 7401355 Suction/Pressure Foot Switch....................................... 6-2
6.3. Troubleshooting Guide ........................................................................................................ 6-3
Section 7 Technical Information ..................................................................................................... 7-1
7.1. Cabinet Pump Compartment Components ........................................................................ 7-1
7.2. Cabinet Schematic ............................................................................................................... 7-2
Section 9 Technical Data ................................................................................................................ 9-1
Appendix A-1 Cabinet Model/Type ................................................................................................. 9-2
Appendix A-2 List of Accessories .................................................................................................. 9-3
Appendix A-3 Test Standards ......................................................................................................... 9-6

Section 1 Important Safety Instructions
1-1
1.1. Symbol Denitions
This symbol on the product is an attention symbol, alerting the user to read the
Owner’s Manual for important installation, operating instructions or safety information.
This symbol on the product indicates a potential electrical shock hazard and alerts the user to read the
Owner’s Manual for important safety information.
Symbol indicating “not for general waste.” Recycle per the EUROPEAN WASTE ELECTRICAL AND
ELECTRONIC EQUIPMENT (WEEE) DIRECTIVE.
This symbol indicates protective earth ground.
For Professional Use Only.
This symbol means On (power).
This symbol means O󰀨 (power).
This symbol indicates a surface that could be hot to the touch.
This symbol alerts the user that this product emits bright light.
This symbol indicates an explosion hazard.
Symbol indicating do not expose to wetness or high moisture conditions.
This symbol indicates Biological hazard.
2
Symbol indicating Single Use Only. Do not attempt to clean, sterilize or reuse.
Symbol indicating Use By Date.
This symbol indicates keep dry.
Symbol indicating an accessible location on or within the cabinet where there is risk that a body part
may become trapped.
This symbol indicated Do Not Push.
!
WARNING
THE SAFETY AND SATISFACTION OF OUR CUSTOMERS AND THEIR PATIENTS
ARE THE HIGHEST PRIORITIES OF DULONG MEDTECH. THIS MANUAL CONTAINS
IMPORTANT INFORMATION REGARDING THE SAFE AND PROPER USE OF THIS
EQUIPMENT AND SHOULD BE READ THOROUGHLY BY ALL OPERATORS PRIOR TO
THEIR FIRST USE OF THE EQUIPMENT. FAILURE TO READ AND UNDERSTAND THIS
MATERIAL COULD RESULT IN INJURY TO PATIENTS OR PERSONNEL OR IN DAMAGE TO
THE EQUIPMENT.

Section 1 Important Safety Instructions
1-2
1.2. Warnings and Cautions
WARNING
!
This symbol indicates a situation in which incorrect handling through disregard of a warning
might result in death or serious personal injury.
CAUTION
!This symbol indicates a situation in which incorrect handling through disregard of a
caution might result in personal injury or may result in damage to property.
NOTICE This symbol indicates a message to avoid property damage or additional information to help
complete a procedure.
WARNING ELECTRICAL SHOCK HAZARD! DISCONNECT ALL ELECTRICAL POWER
PRIOR TO SERVICING CABINET. CONNECT THE MAXI TREATMENT
CABINET ONLY TO A PROPERLY-WIRED GROUNDED RECEPTACLE.
WARNING
EXPLOSION HAZARD! DO NOT USE THE MAXI TREATMENT CABINET IN THE EXPLOSION HAZARD! DO NOT USE THE MAXI TREATMENT CABINET IN THE
PRESENCE OF FLAMMABLE ANESTHETICS OR OTHER FLAMMABLE PRESENCE OF FLAMMABLE ANESTHETICS OR OTHER FLAMMABLE
SUBSTANCES IN COMBINATION WITH AIR, OXYGEN-ENRICHED SUBSTANCES IN COMBINATION WITH AIR, OXYGEN-ENRICHED
ENVIRONMENTS OR NITROUS OXIDE.ENVIRONMENTS OR NITROUS OXIDE.
WARNING
LIQUIDS CAN DAMAGE THE ELECTRONICS INSIDE AND OUTSIDE OF THE
CABINET AND CAUSE AN ELECTRICAL SHOCK HAZARD. PREVENT LIQUIDS
FROM SPILLING ON OR DRIPPING INTO THE CABINET.
WARNING TO AVOID RISK OF ELECTRICAL SHOCK, THIS EQUIPMENT MUST ONLY BE
CONNECTED TO A SUPPLY MAINS WITH PROTECTIVE EARTH GROUND.
WARNING NO MODIFICATIONS TO THE EQUIPMENT ARE ALLOWED WITHOUT
AUTHORIZATION OF THE MANUFACTURER.
WARNING
IF THIS EQUIPMENT IS MODIFIED, APPROPRIATE INSPECTION AND TEST-
ING MUST BE CONDUCTED TO ENSURE CONTINUED SAFE USE OF THE
EQUIPMENT.
WARNING THE CABINET SHALL NOT BE SERVICED OR MAINTAINED WHILE IN USE
WITH A PATIENT.
WARNING
!
IT IS HIGHLY RECOMMENDED THAT THE INSTALLATION OF THIS
EQUIPMENT BE PERFORMED BY QUALIFIED TECHNICIANS. INSTALLATION
BY UNQUALIFIED INDIVIDUALS COULD RESULT IN PERSONAL INJURY.
WARNING TO MINIMIZE THE RISKS DUE TO PINCH POINTS, KEEP ALL OBJECTS AND
BODY PARTS OUT FROM UNDER THE CABINET WHEN TRANSPORTING.
WARNING
!
DO NOT PLUG ANY UNAUTHORIZED COMPONENTS INTO OUTLET STRIP IN
CABINET, AS DOING SO WOULD REQUIRE RE-EVALUTION OF CABINET TO
RELEVANT STANDARDS.
WARNING
!
USE OF THIS EQUIPMENT ADJACENT TO OR STACKED WITH OTHER
EQUIPMENT SHOULD BE AVOIDED BECAUSE IT COULD RESULT IN IM-
PROPER OPERATION. IF SUCH USE IS NECESSARY, THIS EQUIPMENT AND
THE OTHER EQUIPMENT SHOULD BE OBSERVED TO VERIFY THAT THEY
ARE OPERATING NORMALLY.
WARNING
!
USE OF ACCESSORIES AND CABLES OTHER THAN THOSE SPECIFIED OR
PROVIDED BY THE MANUFACTURER OF THIS EQUIPMENT COULD RESULT
IN IMPROPER OPERATION. IF SUCH USE IS NECESSARY, THIS EQUIPMENT
AND THE OTHER EQUIPMENT SHOULD BE OBSERVED TO VERIFY THAT
THEY ARE OPERATING NORMALLY.

Section 1 Important Safety Instructions
1-3
WARNING
!THIS SYSTEM IS INTENDED FOR USE BY HEALTHCARE PROFESSIONALS
ONLY.
WARNING
!
THIS SYSTEM MAY CAUSE RADIO INTERFERENCE OR MAY DISRUPT THE
OPERATION OF NEARBY EQUIPMENT. IT MAY BE NECESSARY TO TAKE
MITIGATION MEASURES, SUCH AS RE-ORIENTING OR RELOCATING SMR
CABINET OR SHIELDING THE LOCATION.
WARNING
!TOO HIGH OF PRESSURE COULD RESULT IN HAZARDOUS OUTPUT FOR
DISPENSING MEDICATIONS.
CAUTION
!
A Hydrophobic Filter is installed in the vacuum line. Failure to replace this lter
regularly (at least once a month) will lead to reduced ow. Extended use of
alcohol or solvents may reduce the e󰀩ciency of the microporous membrane of
the hydrophobic lter. If these chemicals are used frequently, the lter should be
inspected and replaced more often than the recommended time.
CAUTION
!
Non-use of the hydrophobic lter may lead to possible contamination and pump
failure. Global Surgical will not receive or replace any pump in which the
Hydrophobic Filter was not used.
CAUTION
22
Canister is Single Use Only. Do Not attempt to clean, sterilize or reuse canister.
Possible consequences of reuse include: 1.) implosion, 2) uid bypass, and
3) exposure to blood borne pathogens.
CAUTION
!
Canister is Single Use Only, Do Not attempt to clean, sterilize or reuse canister.
Possible consequences of reuse include: 1.) Implosion, 2) Fluid bypass, and
3) Exposure to blood borne pathogens.
CAUTION
!
Care should be used by all personnel coming into contact with suction
equipment. Wear gloves when handling suction equipment. Hand washing is
necessary to prevent the possibility of cross-contamination.
CAUTION Dispose of the disposable suction canister containing medical waste in an
environmentally safe manner per state and federal regulations.
CAUTION
!After moving cabinet to its permanent location, lock the four casters to keep it
from moving.
CAUTION
!DO NOT block the Light Source ventilation slot on the back side of the MAXI
Treatment Cabinet during operation.
CAUTION
!Drawers must be closed before transporting any MAXI Treatment Cabinets.
CAUTION
!The internal power receptacles located inside the cabinet are not for general
use.
CAUTION
!Failure to cut and remove the shipping tape from around the two pumps will
result in damage to the pumps.
CAUTION To reduce the risk of electric shock do not open pump compartment while
master power switch is turned on. Refer servicing to qualied service personnel
CAUTION
!To prevent tipping, push the cabinet from the side not the front or back.
Only open one drawer at a time.
CAUTION
!Before moving cabinet to a di󰀨erent location, remove all loose equipment
from the counter top.

Section 1 Important Safety Instructions
1-4
CAUTION
!Maximum weight for contents of cabinet drawers is 4 lbs per drawer.
CAUTION
!Safe Working Load: 2 KG (4 lbs.) each drawer or shelf or counter surface.
Duty Cycle: 10 min. maximum On Vacuum/Pressure, 10 min. O󰀨.
CAUTION
!
Replacement parts, such as cables, must be purchased through Global Surgical
to ensure proper compliance requirements. Unauthorized use of these items will
void warranty and may cause injury to you, others and/or the equipment.
CAUTION
!
When used in clinical or residential areas near radio or TV units, this equipment
may be subject to radio interference. To avoid adverse electromagnetic
e󰀨ects, do not operate this equipment near RF energy equipment.
CAUTION
!To prevent any potential electromagnetic interference, do not use any kind of
cellular phone near the equipment.

Section 2 Unpacking and Preparation for Use
2-1
!
WARNING
FAILURE TO FOLLOW THESE INSTRUCTIONS WILL RESULT IN DAMAGE TO THIS
SYSTEM OR POSSIBLE INJURY.
!
WARNING
THE BANDS WILL SPRING APART WHEN CUT ON THE SHIPPING BOX.
ENSURE THEY WILL NOT HIT ANYONE OR ANYTHING. EYE PROTECTION SHOULD
BE WORN WHEN REMOVING THE BANDS. WATCH FOR SHARP EDGES.
!
CAUTION Contents are fragile and should be removed carefully.
!
CAUTION Some of the parts may be damaged by knives. Open boxes carefully.
NOTICE Check for damage before discarding the shipping material and notify Dulong Medtech if
shipping damage is observed.
NOTICE Contents are packed in several boxes. Before discarding any packaging, ensure no
components are still within.
NOTICE Save this manual for future reference.
NOTICE
If you have ordered accessories, then some of these may be assembled to the unit while
others are supplied unassembled. Please examine the contents of the box thoroughly. If any
accessories require assembly, then instructions will be included.
All shipping materials should be retained until it has been determined that the unit was not damaged
during shipment.
If damage is discovered, complete the following:
1. Do not refuse shipment.
2. Make a notation on the delivery receipt and inspect the carton for damage.
3. Take pictures of damage to the equipment and to the packaging (if evident).
4. If damage is discovered, leave in original container and request immediate inspection from the carrier
within 3 days.
5. Contact Dulong Medtech Customer Service at 877-695-7687 or [email protected]
If the product is damaged electrically or mechanically and the original packing materials are no longer
available, contact Dulong Medtech Customer Service.
Refer to Section 8 of this manual regarding contact information and proceed as instructed.
For further instructions see “ SMR MAXI Cabinet Unpacking Instructions, document 108-014-011.