Precision Medical Easy Go Vac PM66 Series User manual

USER MANUAL
PM66 Series
PM66Li (Shown)
300 Held Drive Tel: [phone]
Northampton, PA 18067 USA Fax: [phone]
ISO 13485 Certified www.precisionmedical.com
SAVE THESE INSTRUCTIONS
Read this manual before operating the device,
save this manual for future reference.

1
Receiving / Inspection
Remove the Precision Medical, Inc. Easy Go Vac Aspirator from packaging and inspect
for damage. If there is any damage, DO NOT USE and contact your Provider.
Intended Use
The Easy Go Vac Aspirator provides a portable, AC/DC powered medical vacuum source.
It is intended for use in the homecare / healthcare environments.
Only use this Aspirator for its Intended Use.
READ ALL INSTRUCTIONS BEFORE USING
This manual instructs a Professional to install and operate the Easy Go Vac Aspirator.
The Easy Go Vac Aspirator is to be used only by trained professional caregivers in a
home or hospital environment.
The Easy GoVac Aspirator isto be usedonly by adultscapable of readingand understanding
the Instructions of Use written in the appropriate language.
This manual is provided for your training, safety and to prevent damage to the Aspirator.
If you do not understand this manual, DO NOT USE the Aspirator and contact your Provider.
Explanation of Abbreviations
mmHg Millimeters of Mercury l/min Liters per Minute
inHg Inches of Mercury
Contents
Receiving / Inspection........................................................................................................1
Intended Use........................................................................................................................1
Read All Instructions Before Using.................................................................................1
Explanation of Abbreviations ...........................................................................................1
Safety Information - Warnings and Cautions...............................................................2
Specifications ......................................................................................................................4
Guidance and Manufacturer’s Declaration..................................................................5
Component identification................................................................................................. 7
Operating Instructions ......................................................................................................9
Cleaning / Maintenance ................................................................................................. 10
Maintenance....................................................................................................................... 11
Canister Removal/Assembly (800cc Disposable).................................................... 13
Canister Removal/Assembly (1200cc Reusable)...................................................... 14
Inline Filter Replacement................................................................................................ 15
Returns................................................................................................................................ 16
Disposal Instructions ....................................................................................................... 16
Troubleshooting.................................................................................................................17
Accessory / Replacement Parts.................................................................................... 18
Limited Warranty ad Limitation Of Liability ................................................................ 19

2
DANGER Indicates an imminently hazardous situation which, if not
avoided, will result in death or serious injury.
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.
CAUTION Used without the safety alert symbol indicates a potentially
hazardous situation which, if not avoided, may result in
property damage.
PM66 SERIES WITH RESPECT TO ELECTRICAL SHOCK,
FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE
WITH ANSI/AAMI ES606011 2012, 3.1 ed, CAN/CSAC22.2
No. 606011 2014 62NA
Caution! U.S. Federal Law restricts this device to sale by or on
the order of a physician.
This device may contain electrical components that are
hazardous to the environment. DO NOT dispose device into
standard trash. Contact your local waste Management for
disposal of Electronic Equipment.
Operating Instructions Follow Instructions for Use
General Warning Sign General Mandatory Action Sign
Date of manufacture Manufacture
Serial Number Model Number
Type BF applied part Class II Equipment
Push to Activate DO NOT disassemble
Battery Degree of protection against
ingress of solids and/or liquids
Battery Low Alternating Current
Battery Charging Direct Current
Battery Full DC power connection, Positive
Center.
“ON” for part of equipment “OFF” for part of equipment
Single Use
There are no components in this
product made with natural
rubber latex.
MR unsafe – This device
may pose hazards in a
MRI environment
Safety Information - Warnings and Cautions

3
CAUTION
• DO NOT store or operate the Aspirator outside the specified
environmental conditions.
• Patients with special needs may require assistance to operate the
Aspirator.
• Incorrect accessories connected to this device may aect the device flow
performance.
• DO NOT allow Aspirator to exceed Operating or Storage Temperature
specifications.
DANGER
To reduce the risk of Electrocution:
• Always unplug the Aspirator after using, except when battery is being
recharged.
• DO NOT use, place or store the Aspirator where it can fall or be pulled
into a tub, sink, water or other liquids. Unplug from wall immediately.
• DO NOT attempt to repair the Aspirator. Any attempt could result in
electrical shock.
• Caution must be exercised when operating the Aspirator where oxygen is
being administered.
• The Aspirator is not suitable for use in an enriched environment of
flammable anesthetic mixture with air, oxygen or nitrous oxide.
The PM66 Series Aspirators meet the requirements of IEC 60601-1-2 and are
considered safe from producing electromagnetic interference with other devices
when used normally in accordance with their intended use. Should the aspirator
cause any interference, try repositioning it or moving it to another location.
WARNING
To reduce risk of burns, electrocution, fire, or injury to persons:
• Close supervision is necessary when this Aspirator is used by, on, or near
children or patients with special needs.
• Use this Aspirator only for its "Intended Use" as described in this manual.
• Use of accessories and connecting parts not designed for this Aspirator
may aect performance and/or cause damage to the device.
• DO NOT use if the Aspirator has been damaged.
• DO NOT clean the Aspirator with harsh or flammable chemicals.
• If the Aspirator tubing becomes occluded against patient’s tissue,
powering o the device may not release tubing.
• No modifications to this device are allowed.
• The negative pressure of the unit must be checked by occluding the
end of the suction tubing before attaching it to the suction catheter, and
prior to each suctioning event. Suction pressure should be set as low as
possible to be eective.
• The connection of high vacuum / high flow devices to low flow
accessories has the potential to harm the patient.

4
Specifications
For technical specifications contact Precision Medical, Inc.
or visit www.precisionmedical.com
Suction Canister: 800ml/1200ml Max Volume - Lid has a float shut
o valve that protects the Aspirator from overfill.
Vacuum is not to exceed 25 inHg (635 mmHg)
Patient Tubing: 1/4 in. ID Non-Conductive PVC tubing, 6 ft. long,
with 1/4 in.- 3/8 in. ID female connectors
Inlet Filter: Inline, Bacterial Filter (included)
Inline, Hydrophobic Filter (optional)
Operating Vacuum Range (running on AC power):
PM66Li: ~50 to ≥ 550 mmHg (1.96 to ≥ 21.6 inHg)
PM66-200: ~10 to ≤ 210 mmHg (0.394 to ≤ 8.26 inHg)
Electrical:
Car Charger (DC): 12 Volts, 1.8 Amps
Household Current (AC): 100 - 240 Volts, 50-60 Hz, 0.60 - 0.25 Amps, 60 Watts
Internal Battery Type:
PM66Li: 14.8 Volt, 4 cell Lithium Ion
PM66-200: 11.1 VDC, 3 Cell Lithium Ion
Operating Temperature Range: 0°F to 122°F (-18°C to 50°C)
Storage / Transport Requirements:
Temperature Range: -40°F to 160°F (-40°C to 71-°C)
Maximum Humidity: 95% Noncondensing
Duty Cycle: 15 Min ON / 15 Min OFF / within a 2 Hour cycle
Run Time (using internal battery):
PM66Li: approx 1 hour
PM66-200: approx 2 hours
Charge Time: 2-3 hours
Specifications are subject to change without prior notice..

5
Guidance and Manufacturer’s Declaration –
Emissions All Equipment and Systems
This device is intended for use in the electromagnetic environment specified below. The
customer or user of this device should assure that it is used in such an environment.
The PM66 Series Aspirators meet the requirements of IEC 60601-1-2 and are considered
safe from producing electromagnetic interference with other devices when used normally
in accordance with their intended use. Should the aspirator cause any interference, try
repositioning it or moving it to another location.
Emissions Test Compliance Electromagnetic Enforcement – Guidance
RF Emissions CISPR 11 Group 1 This device 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 Radiated and
Conducted Emissions
This device is suitable for use in all establishments including domestic,
and those directly connected to the public low-voltage power supply
network that supplies buildings used for domestic purposes.
Harmonics IEC 61000-3-2 Class A
Flicker IEC 61000-3-3 Complies
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment - Guidance
Electrostatic Discharge
(ESD) IEC 61000-4-2
±8kV contact
±15kV air
±8kV contact
±15kV air
Floors should be wood, concrete or ceramic
tile. If floors are synthetic, the relative humidity
should be at least 30%.
Electrical Fast Transient/
burst IEC 61000-4-4
±2kV on AC Mains ±2kV on AC Mains Mains power quality should be that of a typical
commercial or hospital environment.
Surge IEC 61000-4-5 ±1kV Dierential
±1kV Common
±1kV Dierential
±1kV Common
Mains power quality should be that of a typical
commercial or hospital environment.
Voltage dips, short
interruptions and voltage
variations on power supply
input lines IEC 61000-4-11
>95% Dip for 0.5
Cycle
60% Dip for 5 Cycles
30% Dip for 25 Cycles
>95% Dip for 5
Second
>95% Dip for 0.5
Cycle
60% Dip for 5
Cycles
30% Dip for 25
Cycles
>95% Dip for 5
Second
Mains power quality should be that of a
typical commercial or hospital environment.
If the user of this device requires continued
operation during power mains interruptions, it is
recommended that the device be powered from
an uninterruptible power supply or battery.
Power Frequency 50/60Hz
Magnetic Field IEC
61000-4-8
30A/m 30A/m Power frequency magnetic fields should be that
of a typical location in a typical commercial or
hospital environment.
Conducted RF IEC
61000-4-6
6 Vrms from
150 kHz to 80 MHz
6 Vrms from
150 kHz to 80 MHz
Portable and mobile RF communications
equipment should be separated from the device
by no less than the recommended separation
distances calculated/listed below: D=(3.5/V1)√P
Radiated RF IEC 61000-4-3 10 V/m
80 MHz to 2.7 GHz
E1 = 10 V/m D= (3.5/E1) √P 80 to 800 MHz D=(7/E1)√P 800
MHz to 2.5 GHz Where P is the maximum power
rating 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

6
For transmitters rated at a maximum output power not listed above, the recommended separation distance D in meters (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
aected by absorption and reflection from structures, objects, and people
Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and this device. This
device and system are NOT Life-Supporting
This device is intended for use in the electromagnetic environment in which radiated disturbances are controlled. The
customer or user of this device can help prevent electromagnetic interference by maintaining a minimum distance between
portable and mobile RF Communications Equipment and the device as recommended below, according to the maximum output
power of the communications equipment
Maximum Output Power
(Watts)
Recommended Separation Distances for the device (meters)
150 kHz to 80 MHz
D=(1.1667)√P
80 to 800MHz
D=(1.1667)√P
800 MHz to 2.5 GHz D=(2.3333)√
0.01 0.11667 0.11667 0.23333
0.1 0.36894 0.36894 0.73785
1 1.1667 1.1667 2.3333
10 3.6894 3.6894 7.3785
100 11.667 11.667 23.333
For transmitters rated at a maximum output power not listed above, the recommended separation distance D in meters (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
aected by absorption and reflection from structures, objects, and people

7
Component Identification
CAUTION
If for any reason any label becomes illegible or lost, contact Precision Medical, Inc.
Vacuum Control Knob
1200ml Suction
Canister
(Built in overfill
protection device)
800ml Suction
Canister
(Built in overfill
protection device)
Vacuum
Gauge
Power
Source
Indicator
Charge
Status
Indicator
Battery
Level
Indicator
Exhaust Vents
On/O
Switch
Patient Port
Patient Port
Filter
Filter
External DC
Connector
(if equipped)
AC Connector
with 1200cc Reusable Canister
with 800cc Disposable Canister

8
Power Source
When light is GREEN the indicated power source is
being used.
Charge Status (if equipped)
LOW - The power switch is ON, AC not plugged in and
light is AMBER, the Aspirator Internal Battery requires
charging.
CHARGING - The power switch is OFF, AC is plugged
in and light is AMBER, the Aspirator is in the charging
process.
FULL - The power switch is OFF, AC is plugged in and
light is GREEN, the Aspirator Battery is fully charged.
Battery Level (Li model only)
Push to check battery level
GREEN - Level is Good
AMBER - Level is getting Low
RED - Recharge required
PM66Li (Lithium Ion) PM66 200 (Lithium Ion)

9
1b. Charge Device - Internal Battery
1a. DC outlet and connector
2. Connect suction tubing to canister
4. Block suction tubing
5. Adjust knob to prescribed
vacuum level on gauge
3. Power “ON”
Block end to set
vacuum level
Push button
Operating Instructions
Plug into
wall outlet
DC outlet
Power
“OFF”
Full charge
2 to 3 hrs.
Push together
Ensure all connections are tight.
6. Perform Procedure
Connect patient suction
attachment/perform procedure
DC connector
1. Connect to external power
source (AC or DC)
or
DC
AC
Device may be used while conncected to AC
PM66Li, PM66S and PM66-200 models only

10
Device in carry bag
7. Power “OFF” when procedure
completed Push button
Operating Instructions (continued)
CAUTION
• Verify battery charge level prior to use.
• Charging Light is on when Aspirator is plugged in and is in the
“OFF” ( ) position only.
• If automatic shut o occurs during battery operation, the Aspirator cannot
be restarted until the battery has been recharged or until the Aspirator is
connected to either of the external power source options (AC or DC).
WARNING
Operating Aspirator after Amber Low Battery Light has been on
continuously, will cause automatic shut down.
Cleaning / Maintenance
WARNING
• Turn the Aspirator “OFF” ( ) and disconnect from any external power
source before cleaning.
• DO NOT clean the Aspirator with Alcohol, Acetone or other solvents.
CAUTION
• Tubing is single patient use only. DO NOT clean.
• Canister is single patient use only.

11
Maintenance
Vacuum/Flow verification should be checked by the device provider as
necessary - Recommended annually or between patients.
Cleaning Instructions
Device with Disposable 800cc Collection Canister
Reference AARC Clinical Practice Guideline - Suctioning of the Patient in the
Home, section HCS 13.0 INFECTION CONTROL
Preparation
1. Shut o device using power switch and allow vacuum to drop. Disconnect
any external power.
2. Disconnect tubing and remove canister from holder.
3. Carefully remove lid and empty contents.
NOTE: Canister should be emptied and cleaned after each use.
WARNING
To prevent possible risk of infection from contaminated cleaning/disinfection
solutions, always prepare fresh solution for each cleaning cycle and discard
solution after each use.
The disposable collection canister and lid are meant for single-patient use.
1. Remove Inlet Adaptor assembly from canister lid and set aside.
NOTE: Filter MUST NOT GET WET. The filter material cannot be cleaned.
2. Remove canister lid, wash in warm water/dishwashing solution. Rinse with
clean, warm water.
3. Soak canister and lid in 1 part vinegar (≥5% acetic acid concentration) to
3 parts water (131°F-149°F/55°C-65°C) solution for 60 minutes. Rinse with
clean with warm water and air dry.
4. Place canister lid back on canister and reinstall Inlet Adaptor assembly.
NOTE: If replacing canister and lid with new, transfer Inlet Adaptor assembly
from old canister to new. Do not reuse old canister lid.
Cleaning Instructions
Device with Reusable 1200cc Collection Canister
Reference AARC Clinical Practice Guideline - Suctioning of the Patient in the
Home, section HCS 13.0 INFECTION CONTROL
Preparation
1. Shut o device using power switch and allow vacuum to drop. Disconnect
any external power.
2. Disconnect tubing and remove canister from holder.
3. Carefully remove lid and empty contents.
NOTE: Canister should be emptied and cleaned after each use.
1. Remove Filter and set aside.
NOTE: Filter MUST NOT GET WET. The filter material cannot be cleaned.

12
2. Wash canister, lid, o-ring, and overflow valve in a solution of warm water
with a mild, liquid detergent (e.g. Dawn or Palmolive) and rinse with clean,
warm tap water.
3. For single patient use: After washing, disinfect using one of the following
method:
Soak in 1 part vinegar (≥5% acetic acid concentration) to 3 parts water
(131°F-149°F/55°C-65°C) solution for 60 minutes. Rinse with clean, warm
water and air dry in a clean environment.
Suction Device (single-patient use)
1. With the power switch in the “O” position, disconnect the PM66PED
EasyGo Vac from all external power sources.
2. Wipe the housing with a clean cloth and any commercial
(bacterial-germicidal) disinfectant.
CAUTION
Do not submerge in water as this will result in damage to the vacuum pump.
NOTE: Do not use any cleaners or disinfectants that contain ammonia,
benzene and/or acetone to clean the device.
Suction Device (multi-patient use)
1. Dispose of all accessory components that are not suitable for reuse, i.e.,
collection canister, filter, tubing and carrying case.
2. With the power switch in the “O” position, disconnect the PM66PED
EasyGo Vac from all external power sources.
3. Visually inspect device for any damage, missing parts, etc.
4. Wipe the housing with a clean cloth and a commercial (bacterial-germicidal)
disinfectant.
5. Replace all accessory components, i.e., collection canister, filter and tubing
with new.
CAUTION
Do not submerge in water as this will result in damage to the vacuum pump.
NOTE: Do not use any cleaners or disinfectants that contain ammonia,
benzene and/or acetone to clean the device.

13
Canister Removal/Assembly (800cc Disposable)
1. Push tabs to release canister
3. Remove lid, empty & clean as instructed in
Cleaning / Maintenance section
5. Place canister on base
7. Push together until they engage (click)
2. Pull canister away from device
4. Reinstall lid securely
6. Align canister assembly with inlet port and
locking tabs with openings on device
8. Correctly reassembled

14
Canister Removal/Assembly (1200cc Reusable)
1. Grasp filter and pull apart
3. Remove lid, empty & clean
5. Align indicators on lid and canister
7. Align with port & push together
2. Tilt o base to remove
4. Place lid on canister
6. Tilt and place canister on device base
8. Correctly installed canister is level

15
800cc Disposable Canister Inlet Adaptor Kit
1200cc Reusable Canister
Inline Filter Replacement
CAUTION
• When installing inline filter be sure the side that has small nubs and says “OUT” is
facing toward inlet port on device.
• Filter cannot be cleaned. If it becomes contaminated or clogged, it must be replaced.
Slightly twist
and pull up
Elbow Elbow
Inline Filter
“OUT” toward device
(side with nubs)
“OUT” toward device
(side with nubs)
Inlet Port
Canister Adaptor
Inlet Adaptor Kit
assembled
Nubs
“OUT”
To remove filter: Pull apart
To install: Push together

16
Returns
Returned products require a Returned Goods Authorization (RGA) number, contact
Precision Medical, Inc. All returns must be properly packaged to prevent shipping
damage. Precision Medical, Inc. will not be responsible for goods damaged in
transit. Refer to Precision Medical, Inc. Return Policy available on the Internet,
www.precisionmedical.com. Precision Medical will NOT repair contaminated
devices (biohazard).
Disposal Instructions
Dispose of Biohazard waste as described by your Healthcare Professional or
Healthcare Facility protocol.
WARNING
• The Aspirator may contain an internal battery. Batteries contain materials
which can contaminate the environment when improperly disposed of.
Dispose of the Aspirator in accordance with local regulations.
• If Aspirator is used for treatment of infectious disease, consult your
Physician or Healthcare Professional for recommended procedures for
proper disposal.
• This device may contain electrical components that are hazardous to the
environment. DO NOT dispose device into standard trash. Contact your
local waste Management for disposal of Electronic Equipment.

17
Troubleshooting
If the Aspirator fails to function, consult this Troubleshooting section. If the
problem cannot be corrected, consult your Provider.
There are no user serviceable parts inside this device. DO NOT open case.
Problem Probable Cause Remedy
Aspirator will
not operate on
battery
1. On/O Switch in “OFF”
position
2. Battery not charged
(Low battery light on)
1. On/O Switch to “ON’’
position
2. •Recharge battery
• If battery will not charge,
contact your Provider
Aspirator will not
operate when
connected to AC
Power Source
1. On/O Switch in “OFF”
position
2. AC Power Cord not
connected
1. On/O Switch to “ON”
position
2. Check connection at both
AC Power Source and
Aspirator
Aspirator will not
operate when
connected to
Auto DC Power
Cord
1. On/O Switch in “OFF”
position
2. Car not turned on.
3. Auto DC Power Cord not
connected properly
4. Defective auto power port
receptacle
5. Defective Auto DC Power
Cord
1. On/O Switch to “ON”
position
2. Turn on car to activate it’s
DC outlet
3. Check connections at both
ends of cord
4. Connect to a known
working auto power port
5. Contact your Provider
Battery will not
charge
1. Not connected to AC
power source
2. Defective battery
1. Connect to AC power source
2. Contact your Provider
Unable to achieve
desired vacuum
setting
1. Filter not connected
properly
2. Filter not installed
correctly.
3. Suction Canister not
connected properly
4. Defective Suction Canister
5. Defective Aspirator
6. Suction Tubing Leaks
1. Confirm and tighten
connections
2. Confirm orientation of filter.
3. Confirm and tighten
connections
4. Replace Suction Canister
5. Contact your Provider
6. Replace Suction Tubing
No Suction 1. Collection Canister
overflow mechanism failed
2. Hydrophobic Filter blocked
by fluid.
3. Collection Canister full
1. Replace Collection Canister
2. Replace Filter
3. Empty Collection Canister
Aspirator stops
running, power
switch “ON”,
battery or AC
power applied
1. Device overheating 1. Power “OFF” device and
allow cooling.
2. Ensure device has adequate
ventilation. Ensure vents are
not blocked.

18
Accessory / Replacement Parts
Only use accessories designed for use with this Aspirator.
• Use tubing intended for suction only.
• Use Collection Canisters designed for use with this Aspirator only.
• Use Precision Medical: Inlet Filter, External AC & DC Power Cord &
Carry Bag Only
Description Part #
*Inlet Filter (Hydrophobic) 506851
Inlet Filter (Bacterial) 507754
800cc Canister, (Case-10 ea.) 502519-10
800cc Inlet Adapter Kit 507521
1200cc Canister 507522
Patient Suction Tubing 1955
Carry Bag 507263
AC Power Cord 506961
Auto DC Power Cord 507213
*Hydrophobic Filter will provide higher level of protection, stopping
the egress of liquid into the device, if canister overfill protection should fail.

507099rev5 11/18 (??m) Printed in USA
Limited Warranty And Limitation Of Liability
Precision Medical, Inc. warrants that Easy Go Vac Aspirator
(the Product) and the following component parts thereof will
be free of defects in workmanship and/or material for the
following periods:
Easy Go Vac Aspirator Two (2) years from shipment
Battery Six (6) months from shipment
Should any failure to conform to this warranty appear within the
applicable period, Precision Medical, Inc. shall, upon written
notification thereof and substantiation that the goods have
been stored, installed, maintained and operated in accordance
with Precision Medical, Inc.’s instructions and standard industry
practice, and that no modifications, substitutions, or alterations
have been made to the goods, correct such defect by suitable
repair or replacement at its own expense.
ORAL STATEMENTS DO NOT CONSTITUTE WARRANTIES.
The representativesof PrecisionMedical,Inc. oranyretailers are
not authorized to make oral warranties about the merchandise
described in this contract, and any such statements shall not
be relied upon and are not part of the contract for sale. Thus,
this writing is a final, complete and exclusive statement of the
terms of that contract.
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ANY
WARRANTY OF MERCHANTABILITY, FITNESS FOR A
PARTICULAR PURPOSE OR OTHER WARRANTY OF QUALITY,
WHETHER EXPRESS OR IMPLIED.
Precision Medical, Inc. shall not under any circumstances
be liable for special, incidental or consequential damages
including but not limited to lost profits, lost sales, or injury to
person or property. Correction of non-conformities as provided
above shall constitute fulfillment of all liabilities of Precision
Medical, Inc. whether based on contract, negligence, strict
tort or otherwise. Precision Medical, Inc. reserves the right to
discontinue manufacture of any product or change product
materials, designs, or specifications without notice.
Precision Medical, Inc. reserves the right to correct clerical or
typographical errors without penalty.