ActivePure Medical Guardian User manual

READ MANUAL CAREFULLY FOR PROPER USE AND OPTIMAL OPERATION.
14841 Dallas Parkway, Suite 500 | Dallas, TX 75254
ActivePure Medical
™
Healthcare Inspired, Science Powered.
MODEL: F171A (230V)

2
IMPORTANT SAFETY & USE INSTRUCTIONS FOR THE ACTIVEPURE MEDICAL GUARDIAN
Read all instructions before using this device.
Keep out of the reach of children.
• Use only as described in this manual
• This appliance contains a UVC bulb
• Unintended use of the appliance or damage to the housing may result in the escape of dangerous UVC radiation;
UVC radiation may, even in little doses, cause harm to the eyes and skin
• The appliance is not to be used by persons (including children) with reduced physical, sensory, or mental capabilities,
or lack of experience and knowledge, unless they have been given supervision or instruction
• Children being supervised not to play with the appliance
• This appliance can be used by children aged from 8 years and above and persons with reduced physical, sensory, or mental
capabilities or lack of experience and knowledge if they have been given supervision or instruction concerning use of the appliance
in a safe way and understand the hazards involved
• Cleaning and user maintenance shall not be made by children without supervision
• Read the maintenance instructions before opening the front door
• DO NOT attempt to repair or adjust any electrical or mechanical functions of the ActivePure Medical Guardian.
Contact Customer Service for service support at 1.800.572.6241
• This device will automatically turn off when the door is open
• DO NOT use filters other than authorized ActivePure Medical Guardian filters
• DO NOT place or operate device outdoors or on wet surfaces
• DO NOT look directly at the UV light inside unit when operating; eye damage may occur
• DO NOT allow device to be used as a toy; do not permit children to operate device
• DO NOT use with damaged cord or plug; if device is not working as intended, has been dropped, damaged, left outdoors,
or is wet, contact Customer Service for support at 1.800.572.6241
• NEVER pull or carry by cord, use cord as a handle, close door on cord, or pull cord around sharp edges or corners; keep cord away
from heated surfaces
• DO NOT unplug by pulling on cord; to unplug, grasp the plug to remove, not the cord
• NEVER handle plug or device with wet hands
• Keep hair, loose clothing, fingers, and all parts of body away from openings and moving parts
• Always turn off before unplugging
• To avoid electric shock or fire hazards, plug directly into an appropriate electrical outlet (see voltage listed on unit) using cable provided
• To reduce the risk of electrical shock, this device has a grounded plug (with a third prong); this plug will fit in a grounded outlet only one
way; if it does not fit, do not change the plug in any way; do not use adapters; contact a qualified electrician to install the proper outlet
• This device should not be used near the presence of combustible gasses
• Place this device in a location that allows air to move freely into, around and out of the device
SAVE THESE INSTRUCTIONS
Caution
This device should be maintained in accordance with the device Manual to prevent damage or risk of fire.
Warning
• When using an electrical device, basic precautions should always be taken
• To reduce risk of fire, electrical shock, or injury to persons, observe the following:

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First, read this user manual in its entirety to ensure that the ActivePure Medical Guardian device is used as intended. Then plug it in, turn it on to the
appropriate fan setting. The ActivePure Medical Guardian is designed for quiet operation, as not to disturb people in a professional healthcare
environment.
BEFORE YOU BEGIN USING THE ACTIVEPURE MEDICAL GUARDIAN
FILL IN AND SAVE
Locate the serial number of your new ActivePure Medical Guardian and write it
here. Retain it for future reference.
Model No. ______________________________________________________________
Serial No._______________________________________________________________
Date of Purchase_________________________________________________________
Distributor ______________________________________________________________
Distributor’s Office Phone No.______________________________________________
Distributor’s Office Address ________________________________________________
CONTENTS
Important Safety & Use Instructions . . . . . . . . . . . . . . 2
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . 3
Device Description. . . . . . . . . . . . . . . . . . . . . . . 4
Product Features . . . . . . . . . . . . . . . . . . . . . . . 5
Device Specifications . . . . . . . . . . . . . . . . . . . . . 6
Operation. . . . . . . . . . . . . . . . . . . . . . . . . . .6
Treatment Space . . . . . . . . . . . . . . . . . . . . . . . 7
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
General Maintenance Instructions . . . . . . . . . . . . . . . 8
Cleaning/Disinfecting and Filter Replacement Instructions . . . 9
ActivePure Cell Replacement Instructions . . . . . . . . . . . 11
Replacement Parts. . . . . . . . . . . . . . . . . . . . . . 12
FAQs . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Warranty Information . . . . . . . . . . . . . . . . . . . . 13
Device IEC 60601-1-2:2014 EMC Information . . . . . . . . . 14
The ActivePure Medical Guardian, model F171A is a device intended for medical purposes that is used for the reduction of staphylococcus
epidermidis and erwinia herbicola bacteria, MS2 and Phi-X174 viruses and aspergillum niger fungal spores and bacillus globigii bacterial spores
from the air in a temperature-controlled professional healthcare environment of 70~71°F, 40~45% RH.
The ActivePure Medical Guardian, model F171A has demonstrated the reduction of staphylococcus epidermidis and erwinia herbicola, bacteria
MS2 and Phi-X174 viruses and aspergillum niger fungal spores and bacillus globigii bacterial spores under the following conditions;
Organism Type Organism Name Test Temp/RH Exposure Time (m) Avg Log-Reduction
Bacteria Staphylococcus epidermidis 72°F/50% 60 5.95
Bacteria Erwinia herbicola 72°F/50% 60 5.12
Virus MS2 bacteriophage 72°F/50% 60 5.58
Virus Phi-X174 72°F/50% 60 4.19
Fungal spore Aspergillus niger 72°F/50% 60 4.12
Bacterial spore Bacillus globigii 72°F/50% 60 4.22
INTENDED USE
STORAGE AND DISPOSAL
Do not dispose of this product as household waste. Electrical waste and
electronic products should be appropriately recycled as required by
practices established by your local authority.
LR1384

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The ActivePure Medical Guardian, model Number F171A is a free-standing portable device, manufactured in the USA, constructed of aluminum
and steel, dimensionally measures 11.5” W x 26.5” H x 21.0” D and weighs 48 lbs. The device operates using a standard 230 VAC, 50Hz power
source. Power consumption ranges from 1 watt in standby mode to 125 watts on high speed. The device includes: a HEPA filter; multipoint ionizer;
a photocatalyst module consisting of two 10-watt UVGI bulbs operating at a wavelength of 254nm; two pieces of polycarbonate honeycomb
material with a combined surface area of 708 square inches, coated with a TiO2 based catalyst called ActivePure; power switch; circuit board which
controls the device operations and an internal fan to draw air through the device, as shown in the general device design (Figure 1).
Lab test results demonstrated the ActivePure Medical Guardian, model F171A device using ActivePure to expose Staphylococcus epidermis and MS2
bacteriophage to hydroxyl radicals and super ions formed as the result of UV exposure on the photo catalyst, has the ability to destroy the tested bio
organisms on the filter as shown in Table 1 below.
The bio organisms selected, Staphylococcus epidermidis, a bacteria, and MS2 bacteriophage, a virus, would provide a strong challenge against the
ActivePure hydroxyl radicals and super ions exposure.
Photo Catalyst Module
"ActivePure"
Contaminated Air
Carbon FanHEPA
Ion Strip
Contaminated Air
Figure 1
Organism Type Organism Name Test Temp / RH Exposure Time (H) Avg Log – Reduction
Bacteria, gram + Staphylococcus epidermidis 73.2°F / 50% 1 5.77
Virus, RNA MS2 bacteriophage 73.2°F / 50% 72 4.15
Table 1
DEVICE DESCRIPTION

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PRODUCT FEATURES
It is important to be familiar with the components of the ActivePure Medical Guardian. If any components are missing, contact Customer
Service for support at 1.800.572.6241 or email at [e-mail].
HEPA Filter Chamber
(Filter not shown)
Airflow
Input
Door Pull
Handle
ActivePure Cell Power Cord
(Plug not shown)
UNIQUE FEATURES
• Flow-through air design provides less air resistance
• Multi-point ionization creates negatively charged particles which flow out from a series of carbon brushes
• Carbon to remove odors
• Hydrophobic polypropylene pleated media filter designed to reduce airborne contaminants
• Powerful UVGI bulbs
• Photo catalyst module using ActivePure Technology
• 4-Speed fan draws airborne contaminants through the device
• All steel and aluminum construction for durability and long life
• Automatic ambient light sensor automatically dims display in darkened environment
• Safety shutdown which prevents continued device use once filter and/or ActivePure Cell replacement time is reached
• Assembled in the USA
Airflow
Output
On/Off/Speed Control
Front Panel
Back
Panel

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OPERATION
DEVICE SPECIFICATIONS
MODEL: F171A
Operation Voltage: 230 VAC, 50 Hz; 0.5 Amp
Power Button Function: ON / 1 / 2 / 3 / 4 / OFF
Operational Indicators:
Green ring – power on, device in operation
Filter change – activates after 180 days of usage
Photocatalyst cell (ActivePure Technology) – activates
after 365 days of usage
Reset Button:
Press and hold power button for 10 seconds to reset
filter and/or cell indicators
Ionizer Voltage: 4.5 ~ 7.0 kV
Negative Ion Output (Avg): 8.73 x 106/ cm3
Treatment Area: 3,000 ft3with ceilings 8 ~ 10 ft
(84.9 m3with ceilings 2.4 m ~ 3.0 m)
Recommended Fan Speed: High
Fan Speeds / Fan Indicators: 4
Whisper | 1 blue bar is illuminated
Low | 2 blue bars are illuminated
Medium | 3 blue bars are illuminated
High | 4 blue bars are illuminated
Nominal Airflow Rate:
Whisper | 90 CFM | 53 m3/h
Low | 100 CFM | 59 m3/h
Medium | 180 CFM | 305 m3/h
High | 300 CFM | 509 m3/h
Nominal Wattage:
Standby 1
Whisper 41
Low 46
Medium 60
High 125
Average Sound (dbA)(i):
Whisper 43
Low 48
Medium 64
High 70
(measured @ 1m from front)
Dimensions:
26.5"H x 11.5"W x 21.0"D
(673mm H x 292mm W x 533mm D)
Weight:
48 lbs.
21.8 kg
Power Cord: 6 ft. (1.8 m)
ActivePure Medical, LLC reserves the
right to change or modify any
specifications without notice. Consult
Activepure.com for the latest device
information or consult Customer
Service at 1.800.572.6241.
Life:
3-years minimum operational life
1. Place the ActivePure Medical Guardian in a location that allows air to move freely into, around, and out of the unit.
Allow 12" of clearance (minimum) around the intake grille to ensure adequate airflow.
DO NOT place the unit:
• Directly on or near soft furnishings (such as bedding or curtains)
• Near sources of heat (such as radiators, fireplaces, or ovens)
• Near combustible gases
• Near water, outdoors, or in a damp area
2. Open the side panel and remove the filter from the plastic wrapper.
3. Reinstall the filter and close the side panel.
4. Plug the unit into a standard wall outlet.
5. Once the unit is plugged in, push the On/Off/Speed Control button until you reach
the highest appropriate speed.
NOTE: To reduce the fan speed, cycle through the "Fan Speeds" (page 9) by continuing to push the
On/Off/Speed Control button until the desired speed is reached.
On/Off/Speed Control
(The green light illuminates when the power is on.)

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The ActivePure Medical Guardian, model F171A is a device intended for medical purposes that is used in professional healthcare environments.
The device is designed to treat a space approximately 3,000 cubic feet that would have 8’ to 10’ ceilings. Recommended mode of action is
to operate the device on the highest speed possible continuously. The device recirculates ambient air continuously through the device where
the filter using straining and attraction reduces airborne contaminants from the air. Hydroxyl radicals and super ions created by the photo
catalyst ActivePure are mixed with the contaminant reduced air which then enters the treatment space. The ActivePure photo catalyst reduces
the viability of microorganisms 4-6 log such as Staphylococcus epidermidis and MS2 as tested, shown in Table 3. Larger spaces or operating
on lower fan speeds may require multiple devices. Operational guidelines are provided to users in the form of an Owner’s Manual. The length
of time required to reach optimal reduction varies as a function of space volume and the dynamics of what occurs within the treatment space
including:
• Degree of contaminants in the air or being introduce by activities in the space
• Movement of people or equipment within the space
• Rates of ventilation
The device is intended to result in a 4-6 log reduction of airborne microorganisms from initial concentrations in 60 minutes as shown in Table 1.
The ActivePure Medical Guardian, model F171A is not a sterile device and is not intended to create a sterile environment.
Organism Type Organism Name Initial Load of
Microorganisms
Avg Log-Reduction after
60 minutes
Bacteria (gram +) Staphylococcus epidermidis 2.6e5cfu/L 5.95
Bacteria (gram -) Erwinia herbicola 1.9e5cfu/L 5.12
Virus (RNA) MS2 8.1e5cfu/L 5.58
Virus (DNA) Phi-X174 7.63e3cfu/L 4.19
Fungal spore Aspergillus niger 2.61e4cfu/L 4.12
Virus (DNA) Baillus globigii 7.95e5cfu/L 4.22
Fan Speed CFM of Air Movement Cubic Feet Air
Movement in 1 Hour
Air Exchanges per Hour
based on
3,000 ft3
Whisper 90 5,400 1.8
Low 100 6,000 2.0
Medium 180 10,800 3.6
High 300 18,000 6.0
Table 1
Table 2
Table 3
The information on the device CFM performance and air exchanges for the different speed settings is shown in Table 2, to illustrate the influence of
treatment space to air exchanges on different fan speeds. These are provided to assist in determining the number of devices or fan speed settings
necessary for a given space.
Organism Type Organism Name Test Temp / RH Exposure
Time (H)
Avg
Log–Reduction
Bacteria, gram + Staphylococcus epidermidis 73.2°F / 50% 1 5.77
Virus, RNA MS2 bacteriophage 73.2°F / 50% 72 4.15
TREATMENT SPACE

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There are four fan speed settings on the ActivePure Medical Guardian:
1. Whisper (one blue light illuminated)
2. Low (two blue lights illuminated)
3. Medium (three blue lights illuminated)
4. High (four blue lights illuminated)
NOTE: The safety switch automatically turns the power off when the door is open.
For best results, run your ActivePure Medical Guardian 24 hours a day, 7 days a week.
On/Off/Speed Control
(The green light illuminates when the power is on.)
The ActivePure Medical Guardian is designed to reduce airborne contaminants with minimal maintenance.
Filter: The ActivePure Medical Guardian HEPA Filter is replaced when the change filter light illuminates after
180 days (approx 6 months) of use.
Cell Module: The ActivePure Medical Guardian ActivePure Cell is replaced when the change cell light
illuminates after 365 days (1 year) of use.
The ActivePure Medical Guardian has a safety shutdown feature to ensure the filter and/or cell replacement is
performed at the appropriate times. When the filter and/or cell replacement time is reached, the appropriate
LED indicator will illuminate. However, if the replacement indicator(s) are ignored or if the one or both LED's
fail to illuminate, by design the device will shut down 3 days of operation after reaching the replacement time.
This is to ensure the device does not continue to operate with a filter and/or cell past its stated life.
Cabinet: Wipe the exterior of the cabinet with a clean, soft cloth as needed to remove finger prints,
smudges, etc. Clean and disinfect device after each filter change as detailed in the Cleaning/
Disinfecting and Filter Replacement Instructions.
Important Points:
• Always unplug device before cleaning
• Never use gasoline, chemical solvents or any type of corrosive material to prevent damage to
the device
• Use genuine ActivePure Medical parts to maintain the warranty (See Warranty on Page 11)
GENERAL MAINTENANCE INSTRUCTIONS
SETTINGS
Caution
Disconnect power before servicing.

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The ActivePure Medical Guardian, model F171A is a device intended for medical purposes that is used for the reduction of
staphylococcus epidermidis and erwinia herbicola bacteria, MS2 and Phi-X174 viruses and aspergillum niger fungal spores and bacillus
globigii bacterial spores from the air in a temperature-controlled professional healthcare environment of 70~71°F, 40~45%RH.
The following instructions cover device cleaning, disinfecting and replacement of the filter. Thoroughly read all of the instructions before
starting. It is recommended to clean and disinfect the device each time the filter is replaced or when device becomes visibly soiled.
FILTER REPLACEMENT
Metrex CaviWipes are required to clean the device when replacing the filter, but they are not provided with the unit or filter.
Step 1: Always disconnect (unplug) device from electrical power source before cleaning, disinfecting or replacing the filter.
Step 2: If necessary, relocate the device to an appropriate area to perform the cleaning, disinfecting and filter replacement. It is not
recommended to perform these tasks in areas such as patient room, operating room, examination room, etc., where patient
exposure may occur.
Step 3: Open the replacement filter carton which includes the following items inside.
• 1 replacement filter in a sealed wrapper
• 1 disposable surgical mask
• 1 pair disposable latex free gloves, large
• 1 disposable 8-quadrant wiping cloth
• 1 large plastic bag
• 1 red bio hazard sticker
• 1 plastic bag seal
• 1 printed copy of instruction for use, cleaning, disinfecting, filter replacement sheet
Step 4: Before removing and handling the used filter, put on the disposable mask and gloves.
Step 5: Slide (remove) the used filter from the device, placing it inside the large plastic bag provided for disposal, then set it aside.
Step 6: Use Metrex CaviWipes to clean the device. These are NOT provided with the device or
replacement filter.
NOTE: Metrex CaviWipes are required to clean the device when replacing the filter, but they are not provided
with the unit or filter.
Step 7: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “A”. Wipe the CaviWipe
over the surface area, thoroughly wetting the soil. Then using hand pressure rub the wipe over the
surface until soil is no longer visible on this part of the device. If soil is heavy or is still visible, repeat
step with a new CaviWipe until soil is no longer visible.
Step 8: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “B”. Wipe the CaviWipe
over the surface area, thoroughly wetting the soil. Then using hand pressure rub the wipe over the
surface until soil is no longer visible on this part of the device. If soil is heavy or is still visible, repeat
step with a new CaviWipe until soil is no longer visible.
Step 9: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “C”. Wipe the CaviWipe
over the surface area, thoroughly wetting the soil. Then using hand pressure rub the wipe over the
surface until soil is no longer visible on this part of the device. If soil is heavy or is still visible, repeat
step with a new CaviWipe until soil is no longer visible.
1
2
3
4
5
A
B
C
CLEANING/DISINFECTING AND FILTER REPLACEMENT INSTRUCTIONS

10
Step 10: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “C”. Wipe the CaviWipe
over the surface area, thoroughly wetting the soil. Then using hand pressure rub the wipe over the
surface until soil is no longer visible on this part of the device. If soil is heavy or is still visible, repeat
step with a new CaviWipe until soil is no longer visible.
Step 11: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “E”. Wipe the CaviWipe
over the surface area, thoroughly wetting the soil. Wait 1 minute, then using hand pressure rub the
wipe over the surface until soil is no longer visible on this part of the device. If soil is heavy or is still
visible, repeat step with a new CaviWipe until soil is no longer visible.
Step 12: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “F”. Wipe the CaviWipe
over the surface area, thoroughly wetting the soil. Wait 1 minute, then using hand pressure rub the
wipe over the surface until soil is no longer visible on this part of the device. If soil is heavy or is still
visible, repeat step with a new CaviWipe until soil is no longer visible.
Step 13: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “G”. Wipe the
CaviWipe over the surface area, thoroughly wetting the soil. Wait 1 minute, then using
hand pressure rub the wipe over the surface until soil is no longer visible on this part of
the device. If soil is heavy or is still visible, repeat step with a new CaviWipe until soil is no
longer visible.
Step 14: Remove a Metrex CaviWipe from its package. Begin by cleaning the surface “H”. Wipe the
CaviWipe over the surface area, thoroughly wetting the soil. Wait 1 minute, then using
hand pressure rub the wipe over the surface until soil is no longer visible on this part of
the device. If soil is heavy or is still visible, repeat step with a new CaviWipe until soil is no
longer visible.
Step 15: Allow the device to dry, no visible wetting remains. No rinsing is required. With the
device cleaned, it is ready for disinfecting.
DISINFECTING
Disinfectants are typically provided as a concentrate to be mixed with water or ready to use (RTU) with no mixing required. Use Clorox
Healthcare Fuzion Cleaner Disinfectant RTU in a spray bottle. As an RTU product, no mixing is necessary. Clorox recommended disinfectant
wait time is 1 minute with no rinsing required.
In Steps 16 - 24, spray Clorox Healthcare Fuzion Cleaner Disinfectant liberally on each surface until that surface is thoroughly wetted.
Step 16: Take the 8-quadrant wiping cloth from the filter carton, folding it as before so quadrant 1 is showing.
Step 17: Spray disinfecting solution over surface A. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 1. Continue wiping until all solution has been removed.
Step 18: Spray disinfecting solution over surface B. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 2. Continue wiping until all solution has been removed.
Step 19: Spray disinfecting solution over surface C. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 3. Continue wiping until all solution has been removed.
Step 20: Spray disinfecting solution over surface D. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 4. Continue wiping until all solution has been removed
Step 21: Spray disinfecting solution over surface E. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 5. Continue wiping until all solution has been removed.
E
F
GH
C
CLEANING/DISINFECTING AND FILTER REPLACEMENT INSTRUCTIONS (CONT.)

11
Step 22: Spray disinfecting solution over surface F. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 6. Continue wiping until all solution has been removed.
Step 23: Spray disinfecting solution over surface G. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 7. Continue wiping until all solution has been removed.
Step 24: Spray disinfecting solution over surface H. Wait 4 minutes, ± 5 seconds, then thoroughly wipe with the cloth folded to
quadrant 8. Continue wiping until all solution has been removed.
Step 25: When finished, place the disposable mask, gloves and wiping cloth in the large plastic bag with the used filter.
Step 26: Secure the large plastic bag with the provided bag closure and place the red biohazard label on the plastic bag.
Disposal to be in accordance with facility policy.
Step 27: Remove the new filter from its protective wrap and slide (following directions on filter) it into the device. The protective
filter wrap is not a biohazard, so no special handling is required.
Step 28: Allow the device to dry, no visible wetting remains, and no rinsing is required. Plug device in and perform a reset of the filter
change light by pressing and holding the power button for 10 seconds until the filter replace light goes out.
Step 29: The device is now ready to be returned to use.
The ActivePure Medical Guardian, model F171A is a device intended for medical purposes that is used for the reduction of staphylococcus
epidermidis and erwinia herbicola bacteria, MS2 and Phi-X174 viruses and aspergillum niger fungal spores and bacillus globigii bacterial spores
from the air, in a temperature-controlled professional healthcare environment of 70~71°F, 40~45% RH.
The following instructions will permit the device ActivePure Cell to be safely replaced without creating safety concerns in the patient environment.
Step 1: Always disconnect (unplug) device from electrical power source before replacing the ActivePure Cell.
Step 2: If necessary, relocate the device to an appropriate area to perform cell replacement. Do not replace cell in areas such as
patient room, operating room, examination room, etc., where patient exposure may occur.
Step 3: Remove the 4 screws securing the old cell mounting plate on the device.
Step 4: Slide the old cell out of the device and disconnect the two bulb sockets.
Step 5: Open the replacement cell carton and remove the new cell.
Step 6: Place old cell inside the empty new cell carton and dispose of properly.
NOTE: No special handling for contaminants is necessary as the cell is on the exhaust side of the device and does not trap or
contain contaminants.
Step 7: Reattach the two bulb sockets to the new cell.
Step 8: Slide the new cell back inside the device and secure with the 4 screws removed in Step 3.
Step 9: Plug device in and reset the ActivePure Cell Change Light by pressing and holding the power button for 10 seconds until
Cell Change Light goes out.
Step 10: The device is now ready to be returned to its location.
CLEANING/DISINFECTING AND FILTER REPLACEMENT INSTRUCTIONS (CONT.)
ACTIVEPURE CELL REPLACEMENT INSTRUCTIONS

12
REPLACEMENT PARTS (QTY) Part Number
HEPA Filter (1) 49947
ActivePure Cell 49948
Q: When the device is first turned on, the fan runs at a higher speed for a second or two before running on the low setting?
A: The fan on whisper runs very slow so the device provides extra power to the fan for a second or two on start up to ensure the fan is operating.
Q: When I select different fan speeds, why do I hear a clicking sound?
A: The clicking sound is a mechanical relay closing for that speed setting.
Q: When I turn off the device, why does the fan continue to run for a short time?
A: This 3 second delay provides longer fan life.
Q: Why doesn't the display dim immediately when the room gets dark?
A: The automatic dim feature has a brief delay to prevent unnecessary dimming if a shadow momentarily passes in front.
Q: How will I know to change the filter or ActivePure Cell?
A: The device control panel will illuminate a change filter or cell icon when its time to change one or both.
Q: What if I ignore the illuminated icons and decide not to change the filter or cell?
A: The device has a safety feature to prevent the continued use of the device 3 days after it is time to change the filter or cell.
Q: How do I reprocess the device?
A: Follow the instruction inside the user manual, on the website or what comes with a replacement filter. These instruction details the cleaning
and disinfecting procedure.
Q: What if I have question about using the device?
A: Answers may be obtained by calling or emailing Customer Service at [e-mail].
After you replace the filter or ActivePure Cell you will want to reset the indicator light(s). To do so simply press and
hold the power button for 10 seconds. This will reset the filter and/or cell module replacement indicators. Only the
illuminated indicator(s) will be reset when pressing the power button for 10 seconds.
RESETTING FILTER AND/OR ACTIVEPURE PHOTOCATALYST CELL MODULE INDICATORS Press and hold for
10 seconds
If you have questions regarding replacement parts and service, contact Customer Service at 1.800.572.6241.
ACTIVEPURE CELL REPLACEMENT INSTRUCTIONS (CONT.)
FREQUENTLY ASKED QUESTIONS
REPLACEMENT PARTS
Warning
Use only ActivePure Medical, LLC recommended Replacement Parts.

13
WHAT IS COVERED BY THIS WARRANTY
ActivePure Medical, LLC warrants the ActivePure Medical Guardian,
to the original purchaser subject to the conditions below, against
defects in workmanship or material, provided that the products are
registered within one year of purchase and returned to ActivePure
Medical Customer Service within 3 years of purchase.
MAINTENANCE REQUIREMENTS
Failure to use and maintain the ActivePure Medical Guardian
in accordance with the Owner’s Manual will void this warranty,
including but not limited to:
• Replacing your HEPA filters with genuine filters every 180 days (6
months) of use
• Replacing the ActivePure Cell with a genuine ActivePure Cell every
365 days (1 year) of use (proof of change may be required)
HOW TO OBTAIN WARRANTY SERVICE
Customers must contact their authorized sales representative or
Customer Service and provide proof of purchase within the above
time periods. Customer will be responsible to return product to
their authorized sales representative or Customer Service at their
own expense. We will repair or replace and return the device,
without charge and within a reasonable period of time, subject to
the conditions herein, if our examination shall disclose any part to
be defective in workmanship or material. If we, in our discretion,
are unable to repair the device after a reasonable number of
attempts, we will provide either a refund of the purchase price or a
replacement device, at the company’s option.
WHAT IS NOT COVERED BY THIS WARRANTY
This device is intended for use in a professional healthcare
environment only. Ordinary wear and tear shall not be considered
a defect in workmanship or material. These warranties do not
apply for loss or damage caused by accident, fire, abuse, misuse,
modification, misapplication, or by any repairs other than those
provided by an authorized location.
EXCLUSION OF OTHER WARRANTIES AND CONDITIONS
EXCEPT AS PROVIDED HEREIN, ACTIVEPURE MEDICAL, LLC MAKES
NO REPRESENTATION OR WARRANTY OF ANY KIND. ALL OTHER
WARRANTIES OF ANY KIND, EXPRESS OR IMPLIED, ARE HEREBY
EXPRESSLY DISCLAIMED, INCLUDING ANY IMPLIED WARRANTY OF
MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
UNAUTHORIZED CHANNELS & MISSING SERIAL NUMBERS
If a valid serial number is missing from the device, the warranty will
be voided. Genuine devices are permitted to be sold through our
authorized representatives only. Warranties are voided if a device
is purchased through unauthorized channels, this includes websites
that are not authorized to use ActivePure Medical's trademarked
names, images and logos as well as Internet auction sites (e.g. ebay
and Craigslist). The only approved Internet presence for ActivePure
Medical, LLC products is Activepure.com. To confirm warranty
coverage prior to purchasing a device, contact Customer Service at
1.800.572.6241 with the serial number.
LIMITATION OF LIABILITY FOR SPECIAL, INCIDENTAL OR
CONSEQUENTIAL DAMAGES
ACTIVEPURE MEDICAL, LLC SHALL NOT IN ANY CASE BE LIABLE
FOR SPECIAL, INCIDENTAL OR CONSEQUENTIAL DAMAGES
ARISING FROM BREACH OF EXPRESS OR IMPLIED WARRANTIES,
CONDITIONS, GUARANTEES OR REPRESENTATIONS, BREACH OF
CONTRACT, NEGLIGENCE OR ANY OTHER LEGAL THEORY. Such
excluded damages include, but are not limited to, loss of profits or
revenue and loss of the use of the products.
FOR U.S. APPLICATION ONLY
This warranty gives you specific legal rights, and you may also have
other rights which vary from state to state. Some states do not allow
limitations on warranties, or on remedies for breach. In such states,
the above limitations may not apply to you.
PREVENTATIVE MAINTENANCE PROGRAM
Preventative maintenance programs may be available. These
programs help maintain the device’s optimal performance and may
extend the life. To find out if a preventative maintenance program is
available for this device, please contact an authorized representative
or Customer Service at 1.800.572.6241. Terms and conditions will be
all as set forth in the preventative maintenance program documents.
If any provision of this warranty or part thereof is held by a court
of competent jurisdiction to be invalid, illegal or unenforceable,
the validity, legality and enforceability of the remaining provisions
or parts thereof will not in any way be affected or impaired within
the jurisdiction of that court. This entire warranty shall continue to
be valid, legal and enforceable in any jurisdiction where a similar
determination has not been made.
This warranty is provided by:
ActivePure Medical, LLC
14841 Dallas Parkway, Suite 500
Dallas, TX 75254
SERVICE
From time to time, modifications to our devices may occur without
notice. For the latest information, visit Activepure.com/medicalmanuals
or call Customer Service at 1.800.572.6241 or email
at [e-mail].
WARRANTY INFORMATION
Limited Three (3) Year Warranty:
To register your ActivePure Medical Guardian unit, call Customer Service at 1.800.572.6241 or email at [e-mail].

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This device passed each of the 11 tests, as indicated. Immunity test levels performed on the device,
• Electrostatic Discharge Immunity – Tested at 2,4,8 and 15 kV
• Radiated Immunity – Tested 3 V/m (Professional Healthcare) and 10 V/m (Home Healthcare)
• Conducted Immunity – Tested 150 Hz ~ 80 MHz with AM 80% @ 1kHz 3V and 6V
TEST STANDARD
Conducted Emissions (EN 55011, CISPR 11)
Radiated Emissions (EN 55011, CISPR 11)
Harmonics (EN 61000-3-2)
Flicker (EN 61000-3-3: IEC 61000-4-2)
Electrostatic Discharge (EN 61000-4-2: IEC 6100-4-2)
Radiated Immunity (EN 61000-4-3: IEC 61000-4-3)
Fast Transient Burst (EN 61000-4-4: IEC 61000-4-4)
Surges (EN 61000-4-5: IEC 61000-4-5)
Conducted Immunity (EN 61000-4-6: IEC 61000-4-6)
Power Frequency Magnetic Field (EN 61000-4-8: IEC 61000-4-8)
Voltage Dips and Interrupt (EN 61000-4-11: IEC 61000-4-11)
• This device conforms fully to the EMC requirement of IEC 60601-1-2 and is suitable for use in a professional healthcare environment
• This device is not effected by RFID, wireless networks, 2-ways radios, paging systems, etc., as the device does not transmit or receive RF signals
or create EMF beyond the required limits
• Do not use device with an extension cord as unintended EMF may be created
• This device is grounded to prevent electrostatic discharge
• Do not use RF communication or magnetic field generating equipment within 30 cm of the device
• EMC testing shows no conducted or radiated electromagnetic emissions or immunity issues which would be adverse to the patient or operator
The use of this device in a manner other than described in the user manual or a modification of the device could result in
increased electromagnetic emissions or decreased immunity.
If device is operating in an unexpected manner or causing unexpected interference, discontinue using the device, review the
user manual or seek service.
DEVICE IEC 60601-1-2:2014 EMC INFORMATION

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ActivePure Medical, LLC | 14841 Dallas Parkway, Suite 500 | Dallas, TX 75254 | 1.800.572.6241
© ActivePure Medical, LLC. All Rights Reserved
For information regarding the use of this product please call Customer Service.
1.800.572.6241 or Email at [e-mail]
Activepure.com
ActivePure Medical
™
Healthcare Inspired, Science Powered.
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