Bovie Smoke Shark II User manual

Operator’s Manual
© 2020 Bovie Medical Corporation
5115 Ulmerton Road
Clearwater, Florida 33760
US Phone: 1.800.537.2790
Fax: 1.800.323.1640
International Phone: +1 727 384 2323
www.boviemed.com

Smoke Shark II Operator’s Manual: Page 1
MEDICAL – GENERAL MEDICAL EQUIPMENT
AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH ANSI/AAMI ES60601-1:A1:2012, 1:2009/(R)2012
and A2:2010/(R)2012, and CSA CAN/CSA-C22.2 NO. 60601-1:14
E349034
is device complies with Part 15 of the FCC Rules. Operation is subject to the following two
conditions: (1) this device may not cause harmful interference and (2) this device must accept any
interference received, including interference that may cause undesired operation.
Emergo Europe
Prinsessegracht 20
NL-2514 AP The Hague
The Netherlands
Distributed by:
Bovie Medical Corporation
5115 Ulmerton Road
Clearwater, Florida 33760 USA
+1-727-384-2323 Fax +1-727-347-9144
USA 1-800-537-2790
For a period of two (2) years following the date of delivery, Bovie Medical Corporation warrants the Smoke Shark II
against any defects in material or workmanship. Bovie Medical Corporation will repair or replace (at Bovie Medical
Corporation’s option) the same without charge, provided that routine maintenance as specified in this manual has
been performed using replacement parts approved by Bovie Medical Corporation. This warranty is void if the
product is used in a manner or for purposes other than intended.
European Commission requires that any serious incident that has occurred in relation to the device should be
reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is
established.
© 2020 Bovie Medical Corporation
5115 Ulmerton Road
Clearwater, Florida 33760
US Phone: 1.800.537.2790
Fax: 1.800.323.1640
International Phone: +1 727 384 2323
www.boviemed.com
The revision level of this manual is specified by the highest revision letter found on either the
inside front cover or enclosed errata pages (if any).
Manual Number:902958REVF
Bovie® P/N: 23088 r5
12/2020

Smoke Shark II Operator’s Manual: Page 2
Section Title Page
1.0 SYSTEM DESCRIPTION 3
1.1 Introduction
1.2 Inspection
1.3 Operational Information
1.4 Cautions and Warnings
2.0 OPERATING INSTRUCTIONS 11
2.1 System Controls
2.2 Bovie® SF35 Filter Instructions
2.3 Set-up and Operation
2.4 Specications
3.0 MAINTENANCE 20
3.1 General Maintenance Information
3.2 Cleaning
3.3 Periodic Inspection
3.4 Troubleshooting
4.0 CUSTOMER SERVICE 21
4.1 Equipment Return
4.2 Ordering Information
5.0 TERMS & WARRANTY 22
Figure Title Page
1 Control Panel 10
Table of Contents
& List of Illustrations

Smoke Shark II Operator’s Manual: Page 3
1.1 Introduction
Bovie® Smoke Shark II Smoke Evacuation Systems are intended to evacuate and lter surgical
smoke plume and aerosols created by the interface surgical tools with tissue, examples being la-
sers, electrosurgery systems, and ultrasonic devices.
e Smoke Shark II Smoke Evacuation Systems have been designed with a high suction, high ow
rate vacuum motor. e ultra-quiet motor is used to draw the surgical smoke from the surgi-
cal site through the vacuum tubing and into the Bovie® SF35 Filter where the surgical smoke is
processed by a series of lters. A single disposable lter is used to simplify the installation and
removal during lter changes. e lter is completely enclosed to protect the healthcare person-
nel from potential contamination during lter changes. One Bovie® SF35 Filter contains four
dierent stages within to capture the smoke plume.
e rst stage ltration is a prelter whose function is to trap and remove gross particulate and
casual uid.
e second stage ltration is ULPA grade (Ultra Low Penetration Air) lter whose high-tech
patented (U.S. Patent #5874052) design captures particulates and micro-organisms from .1 to .2
microns at an eciency of 99.999%.
e third stage ltration uses the highest grade virgin activated carbon, especially designed for
Bovie Medical Corporation for the removal and adsorption of odors and toxic gases produced
by burning tissues. ese harmful gases may constitute a health hazard to healthcare profession-
als who are subjected to prolonged exposure. e activated carbon used in the Smoke Shark II
Smoke Evacuation Systems preferentially removes toxic organic gases rather than water vapor and
provides optimal odor removal.
e fourth stage ltration is an expanded foam used to trap activated carbon nes from migrating
out of the lter.
e electronic controls on the face panel of the Smoke Shark II Smoke Evacuation System has
been designed “user friendly” and facilitate unit set up and operation. Please refer to Section 2.0
for Operating Instructions.
1.2 Inspection
e Smoke Shark II Smoke Evacuator has been thoroughly tested and inspected before shipment
from the factory. Please check the unit before using it to insure that no damage has occurred
in transit. If damage is evident, please contact Bovie Medical Corporation Customer Service at
1.800.537.2790 (US Only) or +1.727.384.2323 (International)
System Description
Section 1.0

Smoke Shark II Operator’s Manual: Page 4
In addition, please compare the accessories you receive with the standard accessories list below. If
an item is missing, please notify Bovie Medical Corporation Customer Service.
Standard Accessories:
• Operator’s Manual
• Power Cord
• Pneumatic Footswitch
Please contact Bovie Medical Corporation Customer Service to purchase the following
accessories:
• Replacement Filters
• Remote Activation Device
• Hoses, Tubing, Laparoscopic Kits, Adapters, Wands & Other Accessories
1.3 Operational Information
e operational information contained in this section is intended for the customer review of
regulatory issues. e information pertains to the use of the products both domestically and
internationally:
1. The Bovie® Smoke Shark II Smoke Evacuation System(s) complies with electrical
specifications in the following systems:
100/120 VAC 50/60 Hz, 220/240 VAC 50/60 Hz
2. Type of protection against electrical shock: Class I
3. Degree of protection against electric shock; Type CF Applied Part
4. Degree of protection against ingress of water: IPX1
5. Method of sterilization or disinfection recommended by Bovie Medical Corporation:
Unplug Unit. Wipe unit with a damp cloth containing mild disinfectant
solution or soapy water. Wipe dry with a clean cloth. Do not steam sterilize.
6. Degree of safety of application in the presence of flammable anesthetic mixture with air or
with oxygen or nitrous oxide: Not Suitable
7. Mode of operation: Continuous
8. Upon request, Bovie Medical Corporation will provide the following:
Service and Repair Instructions, including Circuit Diagrams and Parts List
9. e fuses on the circuit board are to be serviced by an authorized Bovie Medical Corporation
technician as follows:
100/120 VAC, 50/60 Hz - use T10AH250V Fuse (10 Amp 250 Volt [Slo-Blo]), (F1, F2)
220/240 VAC, 50/60 Hz - use T8.0AH250V Fuse (8 Amp 250 Volt [Slo-blo]), (F1, F2)

Smoke Shark II Operator’s Manual: Page 5
10. This equipment needs special precautions regarding ElectroMagnetic Compatibility
and needs to be installed according to EMC information found in this manual.
11. This equipment utilizes mobile RF communications equipment that can affect medical
electrical equipment.
12. This equipment has been tested and found to comply with the limits for a Class A digital
device, pursuant to Part 15 of the FCC rules. These limits are designed to provide
reasonable protection against harmful interference when the equipment is operated in a
commercial environment. This equipment generates, uses, and can radiate radio frequency
energy and, if not installed and used in accordance with the instruction manual, may cause
harmful interference to radio communications. Operation of this equipment in a
residential area is likely to cause harmful interference in which case the user will be
required to correct the interference at their expense.
13.This equipment operates in the following radio frequency specifications:
14. To isolate equipment from supply mains, unplug the power cord from the appliance inlet on
the unit or receptacle in the wall. Position the equipment to allow for ease of unplugging
power cord.
15. Potential Equalization Conductor: Terminal located on back panel for connection of
potential equalization. Conductor complies with requirements per IEC 60601-1.
RX modulation: Pulse-width coded, AM 100% modulation
TX Frequencies: Manchester encoded,
A = fc =/- 423.75kHz, B = fc +/- 484.29kHz
Low bit: transition A to B
High bit: transition B to A
e Smoke Shark II Smoke Evacuation System(s) and all lters are not intended for contact with
patients.
1.4 Cautions and Warnings
Please note that all Cautions and Warnings should be read and understood before any use of this
equipment.
Please note that all Cautions and Warnings
should be read and understood before any
use of this equipment.

Smoke Shark II Operator’s Manual: Page 6
1.4.1 WARNINGS:
• Read this manual thoroughly, and be familiar with its contents prior to using this equipment.
• Test this equipment prior to a surgical procedure. is product was thoroughly tested at the fac-
tory before shipment.
• Disconnect the unit from the electrical outlet prior to inspecting system components.
• e Smoke Shark II system is only intended and suitable for the applications that are men-
tioned in the operating instructions.
• e smoke evacuator produces a strong vacuum. Adjust the airow and the position of the
inlet end of the wand or tubing to prevent patient injury and to prevent suction of surgical
materials and surgical specimens.
• If the smoke evacuator is activated while the airow is set to a high speed, it may produce a
sudden, strong suction action. Check the airow setting before activating the smoke evacu-
ator to prevent patient injury and to prevent suction of surgical materials and surgical
specimens.
• To maximize patient safety, the tubing or wand should not come into direct contact with
tissue. Otherwise, patient injury may result.
• e Bovie® Smoke Shark II lters and single-use accessories are completely disposable.
Please dispose of according to your local codes or regulations and hospital policy. ese lters
may be disposed of or incinerated, whichever is appropriate for your institution.
• Care should be taken to route the power cord, foot pedal, smoke evacuation tubing, and
Remote Activation Device cable as to not cause a tripping hazard or crimping of cords.
• Do not operate this device in the presence of ammable or explosive gases.
• To avoid risk of Electric Shock, this equipment must only be connected to a supply mains with
protective earth.
• is equipment is intended for use by healthcare professionals only. is equipment 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 the Smoke Shark II or shielding
the location.
• e use of ACCESSORIES other than those specied by Bovie Medical Corporation, or sold by
Bovie® may result in increased emissions or decreased eectiveness of the Smoke Shark II.

Smoke Shark II Operator’s Manual: Page 7
• is equipment should not be used adjacent to or stacked with other equipment and that if
adjacent or stacked use is necessary, the Smoke Shark II should be observed to verify normal
operation in the conguration in which it will be used.
• Refer routine servicing to qualied biomedical technical personnel.
• Changes or modications not expressly approved by Bovie Medical Corporation could void
the user’s authority to operate the equipment.
e warranty on this product is void if any of these warnings are disregarded.
1.4.2 CAUTIONS:
• Federal law (United States of America) restricts this device to be used by, or on the order of a
physician.
• Do not block either the tubing or the lter. If either becomes occluded or signicantly restrict-
ed, the motor/blower may overheat and cause the unit to fail.
• Using any other lter or accessory not supplied by Bovie Medical Corporation may cause
damage and/or cause the system to be inoperable and may void the warranty.
• Care must be exercised in the installation of hoses, adapters and suction canisters. Failure to
follow the procedures outlined in this manual may result in overheating of the motor and may
void the unit warranty.
• is device is not intended for evacuation of uid. If uid is expected to be aspirated to the
Bovie® SF35 Filter, uid collection devices must be installed with the vacuum hose assembly.
Failure to install a uid collection device could cause lter blockage and electrical damage.
• e Bovie® SF35 should be changed according to the life of the lter. e Bovie® SF35 Filter,
used with the Smoke Shark II Smoke Evacuation System(s), should not be used for more the
time specied for each lter. Failure to change the lter may result in decreased eciency and
contamination of the electric motor, vacuum pump, and sound absorbing media within the
unit.
• Do not block either the tubing or the lter during operation. An occlusion or signicant restric
tion may cause the motor to overheat and the unit to stop working.
• e installation of this equipment must be performed such that the intake and exhaust vents
located on the bottom of the system are not obstructed. Failure to properly install the unit may
cause reduced performance, damage and/or cause the system to be inoperable and may void
the warranty.

Smoke Shark II Operator’s Manual: Page 8
• e ambient temperature during operation must be kept between 50°F to 104°F (10°C to
40°C)
• e relative humidity during operation must be kept between 10% to 75%.
• An atmospheric pressure range of 700 hPA to 1,060 hPa.
• Storage environmental ambient temperature 14°F to140°F (-10°C to 60°C).
• Storage environmental relative humidity 10% to 75%.
There are no user serviceable components in the Smoke Shark II Smoke Evacuation
System(s). Refer service to qualied service personnel.
Use only with the power cord provided and always plug into a grounded outlet.

Smoke Shark II Operator’s Manual: Page 9
SYMBOL DESCRIPTION/MEANING
WARNING: DANGEROUS VOLTAGE
WARNING
TYPE CF APPLIED PART.
PROTECTION AGAINST INGRESS OF WATER AS
DETAILED IN IEC 60529.
ALTERNATING CURRENT.
PROTECTIVE EARTH, (GROUND).
EQUIPOTENTIALITY.
DENOTES THE DATE THE EQUIPMENT WAS
MANUFACTURED.
MANUFACTURER
NON-IONIZING RADIATION
MANDATORY: REFER TO INSTRUCTION MANUAL/GUIDE
DANGER- EXPLOSION RISK IF USED WITH
FLAMMABLE ANESTHETICS.
DO NOT USE IF PACKAGING IS DAMAGED OR OPENED.
DO NOT RESTERILIZE
DO NOT REUSE. THIS IS A SINGLE USE DEVICE.
STERILE RADIATION
STERILE ETHYLENE OXIDE
OPERATING TEMPERATURE
LATEX FREE

Smoke Shark II Operator’s Manual: Page 10
Figure 1
Unit Control Panel
SYSTEM MOTOR
POWER BUTTON
SUCTION SPEED BUTTON:
PRESS TO CYCLE THROUGH HIGH,
MEDIUM AND LOW SPEEDS
MOTOR ON LED INDICATOR
STANDBY MODE LED INDICATOR
SERVICE/TROUBLESHOOTING
REQUIRED LED INDICATOR
MOTOR SPEED LED INDICATORS:
Upper Light: HIGH SPEED
Center Light: MEDIUM SPEED
Lower Light: LOW SPEED
CURRENT FILTER LIFE INDICATOR:
AS LIGHTS MOVE FROM GREEN TO
RED, FILTER LIFE DEPLEATS.
REPLACE FILTER WHEN RED.

Smoke Shark II Operator’s Manual: Page 11
2.1 System Controls
e electronic system controls on the Smoke Shark II Smoke Evacuation System(s) are easy to
understand and simple to use. e membrane control panel contains the suction on/o switch,
suction power adjustment, lter life indicator, and service indicator light. See Figure 1.
Note: Please be sure to read all instructions before installing accessories or operating this equip-
ment. Failure to do so may result in damage to the unit and/or personal injury.
• SUCTION ON & Standby
ere is one ON/OFF button on the Smoke Shark II Smoke Evacuation System(s). e suction
ON switch on the electronic membrane control panel is located in the upper right hand corner of
the membrane panel. To power up the machine, connect the supplied power cord to a grounded
outlet and the appliance inlet on the back of the smoke evacuation system. Once power has been
applied, the yellow standby LED will illuminate on the keypad. Press the ON/OFF button on the
membrane panel to illuminate the “fan running” green LED indicating active suction. Place the
unit in “standby” by pressing the suction ON membrane switch to illuminate yellow STANDBY
LED. Turn the system main power o,by unplugging the power cord from the appliance inlet on
the unit or the receptacle in the wall.
• SUCTION CONTROL
(Membrane Control Panel)
e amount of suction may be adjusted by pressing the suction control button. Each time the suc-
tion control button is depressed, the motor speed in increased. Once the suction has reached the
maximum level, depressing the button again will return suction level to lowest setting. e suc-
tion control should be set at the lowest practical setting to completely remove the surgical smoke
from the operative site. Each time the arrow button is pressed, the suction will change to a dier-
ent ow setting (low / medium / high).
• FOOTSWITCH / REMOTE ACTIVATION DEVICE
(Membrane Control Panel)
e Bovie® Smoke Shark II Smoke Evacuation System also comes equipped with a pneumatic
footswitch.
A footswitch or a Remote Activation Device may be added to any system by simply plugging in a
Bovie® activation accessory into the appropriate jack on the front of the unit. When the footswitch
is plugged in, the unit suction may be turned on or o by depressing the footswitch pedal once for
each operation. For directions on using the Remote Activation Device, please see instructions that
accompany that product.
Operating Instructions
Section 2.0

Smoke Shark II Operator’s Manual: Page 12
• FILTER LIFE INDICATOR
(Membrane Control Panel)
e lter life indicator on the membrane control panel provides a visual indication of the status
of the life of the lter in use. e lter life indicator for the Bovie® Smoke Shark II Smoke Evacua-
tion System will automatically adjust according to the ow setting selected.
Low Flow Setting = 35 hours of lter life
Medium Flow Setting = 24 hours of lter life
High Flow Setting = 18 hours of lter life
e Filter Life Indicator is factory set. All lter life timing is automatic.
Reading the Filter Life Indicator:
Install an unused Bovie® SF35 Filter into the system per the installation instructions contained
in this operator’s manual. When the system is turned on, the lter life indicator with light up the
lemost GREEN LED, indicating 100% lter life. e indicator will progress thru subsequent
GREEN LEDs, to an AMBER LED as time elapses and begin ashing RED to indicate that the
lter has expended its useful life and requires replacement.
When the maximum lter life is expended:
The unit will cease operation in six (6) hours or when the unit is manually powered o,
(whichever occurs first). The smoke evacuator will not resume functionality until a new
lter is installed.
• FUSES
(circuit board)
Two T10AH250V [10 AMP] fuses (T8.0AH250V [8 AMP] for 220/240 Bovie® Smoke Shark II
Smoke Evacuation Systems) are located on the circuit board within the housing of the system.
It electrically protects both the system and the operator from damage or injury. If the system is
overheated or if there is an electrical surge in the electrical system, fuses will break and the system
will not operate.
When the Service light illuminates, please contact Bovie Medical Corporation Customer Ser-
vice for system service instructions. (See Section 4.0)

Smoke Shark II Operator’s Manual: Page 13
2.2 Bovie® SF35 Filter Instructions
Note: Before installing or removing any lter, be sure that the system is turned o.
Filter Installation Instructions:
e installation of the Bovie® SF35 Filter into the Bovie® Smoke Shark II Smoke Evacuation
System(s) is quick and simple.
1. Remove the Bovie® SF35 Filter from the shipping box and discard any protective wrapping.
Examine all lters for damage during shipping and storage. Do not install any lter with
visible signs of structural damage.
2. Insert the Bovie® SF35 Filter into the lter receptacle. Be sure that the lter is seated
completely against the bottom of the lter chamber and clip is fully engaged.
WARNING: This device is not intended for evacuation of uid. If uid is expected to be
aspirated using the Bovie® SF35 Filter or the Bovie® Smoke Shark II system, uid collection
devices must be installed with the vacuum hose assembly. Failure to install a uid collection
device may cause lter blockage and/or electrical damage.
Filter Removal Instructions:
1. Aer the Bovie® SF35 Filter has been exhausted and requires changing, turn the smoke
evacuation system o and disconnect any accessory tubing attached to the lter.
2. Depress the lter tab and pull the lter from the smoke evacuation system and dispose of in
accordance with hospital policy. e Bovie® SF35 Filter may be disposed of or incinerated.
3. Wipe unit with a damp cloth containing mild disinfectant solution or soapy water. Wipe dry
with a clean cloth. Do not steam sterilize. Follow the indicated instructions for maintenance
and installation of a new Bovie® SF35 Filter.
CAUTION: Using any other lter or accessory not supplied by Bovie Medical Corporation
may cause damage to the system and/or cause the system to be inoperable and may void the
warranty.
WARNING: The Bovie® SF35 Filter should be changed when the Filter Life Indicator shows
red ashing LED (replace). Failure to change this lter may result in decreased eciency
and contamination of the electric motor, vacuum pump, and sound absorbing media within
the system, or non-operation of smoke evacuator.
Bovie® P/N: SF35
Configuration: Portable or tabletop
Bovie® SF35 Filter - Multi Port Filter: 4-Stage Filtration In One Casing,
(Pre-Filter, ULPA, Carbon, Post-Filter)
Filter(s): ULPA
Particle Size, µm: 0.1 to 0.2 Microns At 99.999% Eciency
Filter Life: Automatic Factory Set Filter Sensor
Filter Life Indicator: Timed Replacement

Smoke Shark II Operator’s Manual: Page 14
2.3 Set-Up and Operation
e operation of the Smoke Shark II Smoke Evacuation System is as follows:
1. Install the Bovie® SF35 Filter.
2. Attach unit power cord to the receptacle on the rear of the system. Plug the pronged power
cord into an appropriate grounded power outlet. Route power cord in such a way as to mini-
mize potential trip hazard by users or patients or pinch hazard that could cause electric shock.
3. Optional: Attach either Remote Activation Device or Footswitch plug into appro-
prate jack on rear or front of machine. Route footswitch or Remote Activation Device cord in
such a way as to minimize potential trip hazard by users or patients or pinch hazard that could
result in unreliable operation.
4. Ensure that the evacuation tubing is fully seated in the inlet of the lter. Route tubing in such a
way as to minimize potential trip hazard by users or patients.
5. Activate the power unit by:
a. Pressing the suction ON/OFF switch on the membrane panel,
b. Depressing and releasing the footswitch (if connected), or
c. Activating either CUT or COAG on the Electrosurgical Pencil (if Remote Activation Device
is connected).
6. Adjust the suction level to the desired setting by pressing the UP arrow button while the unit is
activated. Noise created by the smoke excavation power unit may be minimized by selecting
the lowest vacuum setting that eectively clears the operative eld of surgical smoke.
7. Deactivate the unit by:
a. Pressing the suction ON/OFF switch on the membrane panel,
b. Depressing and releasing the footswitch (if connected), or
c. Releasing either the CUT or COAG button on the Electrosurgical Pencil (If Remote
Activation Device is connected).
8. Replace the Bovie® SF35 Filter when the Filter Life Remaining Scale FLASHES RED (0% Life
Remaining). Failure to change the lter will aect the performance of the system.

Smoke Shark II Operator’s Manual: Page 15
Voltage Available
Motor Watts
Variable Flow Control
Frequency, auto sensed
Display
Noise Level, dBA MAXIMUM
Safety Features
Remote Control Activation
Footswitch Pneumatic
9.5mm
Weight lbs (kg.)
Dimensions (H x W x D) centimeters
Dimensions (H x W x D) inches
6.4mm
3/8”
22mm
Standard Hose I. D. (LPM)
Maximum Flow Setting (lfm-Metric)
1/4”
PERFORMANCE
7/8”
Standard Hose I. D. (CFM)
Maximum Flow Setting
Model Number
Motor Static Suction kPa
(6.5 mm orice)
100/120 VAC, 220/240 VAC
1000 ±10%
Yes
50-60 Hz
Fuse Protection
Service Required
Flow Rate
Filter Status
LED
CE Marked
UL Classied
YES (optional)
Standard
15.2 x 27.9 x 39.4
6 x 11 x 15.5
Smoke Shark II
25.69
2.4 Performance References*
*For reference purposes only
55.0 dBA
10 lbs / (4.3 kgs)
57 LPM
130 LPM
708 LPM
2 CFM
4.5 CFM
25 CFM

Smoke Shark II Operator’s Manual: Page 16
Guidance and manufacturer’s declaration - electromagnetic emissions
2.5 Electromagnetic Compatibility Information per IEC60601-1-2
Table 1
Emissions Test
Voltage Fluctuations/
Flicker Emissions
IEC 61000-3-3
Harmonic
Emissions
IEC 61000-3-2
RF Emissions
CISPR 11
RF Emissions
CISPR 11
Compliance
Class A
Class A
Class A
Group 1
Electromagnetic environment - guidance
Not applicable.
Not applicable.
e model Smoke Shark II is suitable for use in all
establishments, other than domestic establishments and those
directly connected to the public low-voltage power supply
network that supplies buildings used for domestic purposes.
e Smoke Shark II uses RF energy only for its internal
function. erefore, its RF emissions are very low and are not
likely to cause any interference in nearby electronic
equipment.
e Smoke Evacuation System model Smoke Shark II is intended for use in the electromagnetic environment
specied below. e customer or user of the Smoke Shark II should assure that it is used in such an
environment.

Smoke Shark II Operator’s Manual: Page 17
e model Smoke Shark II is intended for use in the electromagnet environment specied below.
Mains power quality should
be that of a typical commercial
or hospital environment. If
the user of the Smoke Shark II
requires continued operation
during power mains interrup-
tions, it is recommended that the
Smoke Shark II be powered by an
uninterruptible power supply or
battery.
<0 % UT
for 0.5 cycle
At 0°, 45°, 90°,
135°, 180°, 225°,
270°, and 315°
<0 % UT
for 1 cycle
70 % UT
for 25/30 cycles
<0 % UT
for 0.5 cycle
At 0°, 45°, 90°,
135°, 180°, 225°,
270°, and 315°
<0 % UT
for 1 cycle
70 % UT
for 25/30 cycles
±8kV contact
±15 kV air
±8kV contact
±15 kV air

Smoke Shark II Operator’s Manual: Page 18
Single phase: at 0°
0° at UT :
250/300 cycles
Single phase: at 0°
0° at UT :
250/300 cycles
30 A/m 30 A/m

Smoke Shark II Operator’s Manual: Page 19
Smoke Shark II.
e model Smoke Shark II is intended for use in the electromagnet environment specied below. e customer
or end user of the Smoke Shark II should assure that it us used in such an environment.
Smoke Shark II
Table 3
Portable and mobile RF communications equipment
should be used no closer to any part of the Smoke Shark
II including cables, than 30 cm (12 in).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey,
should be less than the compliance level in each
frequency range.
80MHz to 2.7
GHz
80% AM at 1kHz
Conducted RF
IEC 61000-4-6
a
b
3 Vrms
0.15MHz -
80MHz
6 Vrms in ISM
bands between
0.15MHz and 80
MHz
80% AM at 1
kHz
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