Bio Compression Systems SC-2004-OC User manual

Quality Medical Products Since 1983
Instrucons For Use
SC-2004-OC, SC-2004FC-OC and SC-2008-OC
Sequenal Circulators
SC-2004-OC
SC-2004FC-OC
SC-2008-OC
SC-2004-OC
&
SC-2004FC-OC
SC-2008-OC

INTENDED USE:
The Sequenal Circulators SC-2004-OC, SC-2004FC-OC /SC-2008-OC are pneumac compres-
sion devices intended for either primary or adjuncve treatment of primary or secondary
lymphedema. The devices are also intended for addional or alternate treatment of venous
insuciency and chronic venous stasis ulcers associated with venous insuciency as well as
general treatment for swelling of the extremies. The devices are intended for both home
and hospital use.
DESCRIPTION OF SYMBOLS:
Refer to Documentaon before using and servicing
CAUTION
Type B - applied part
Electrical shock hazard. Disconnect LINE CORD before servicing; refer servicing to
qualied service personnel
Federal (USA) law restricts this device to sale by or on the order of a physician
IPX0 Without protecon against ingress of water
Class II Protecon
Serial Number
Waste Electrical Goods Recycled
Authorized Representave in the European Community
Conforms with the Medical Device Direcve (93/42/EEC) and has been subject to the con-
formity procedures in the council direcve
Manufacturer
Catalog / Model Number
Keep Dry
Consult instrucons for use
CAUTION: Federal (USA) law restricts this device to sale by or on the order of a physician.

CONTRAINDICATIONS:
Compression is NOT recommended in the following condions:
 Infecons in the limb, including cellulis without appropriate anbioc coverage
 The presence of lymphangiosarcoma
 Deep Vein Thrombosis (DVT)
 Inammatory phlebis or episodes of pulmonary embolism
 Congesve Heart Failure (CHF)
WARNINGS AND PRECAUTIONS
Warnings:
 Pressure sengs should not be changed unless ordered by a physician.
High pressure should be set with cauon on paents with peripheral arterial occlusive
disease.
 Cauon must be exercised for paents with insensive, irritated, sunburned, bruised
or broken skin, or with skin condions such as skin cancer, dermas, eczema, or
psoriasis in/around treatment sites.
 Should changes in skin appearance occur such as blisters, redness, welts,
discoloraon or other noceable changes in the skin, or if burning, itching, increased
swelling should occur, disconnue use and consult with a physician.
 Slip and fall hazard. To avoid the risk of tripping or falling, do not stand or walk while
wearing garments.
Precauons:
 This device is not intended for use during SLEEP.
 Do not aempt to modify this device in any way.
 To prevent the potenal for reverse pressure and retrograde ow, do not
adjust the gradient pressures without a physician’s supervision.
INTRODUCTION
Congratulaons on the purchase of your Bio Compression Systems SC-2004-OC, SC-2004FC-OC
or SC-2008-OC Sequenal Circulator and accompanying garment(s).
DEVICE DESCRIPTION AND OPERATING PRINCIPLE
The SC-2004-OC, SC-2004FC-OC and SC-2008-OC Sequenal Circulators provide gradient pneu-
mac compression for the treatment of lymphedema and associated venous disorders. Sequen-
al gradient compression helps to increase blood ow and move excess lymph away from the
aected area for clearance from the body. These devices can provide sequenal (distal to proxi-
mal) inaon and deaon cycles of compressed air at prescribed pressures.

PACKAGE CONTENTS
1 - SC-2004-OC, SC-2004FC-OC or SC-2008-OC Sequenal Circulator (“pump”)
1 - Instrucons for Use (IFU)
2 - Blocker Bars for use during single garment therapy
1 - Power Cord
0 - Garments (Garments provided separately)
GARMENTS
Cauon: Do not share garments with other users.
Garments are available in sizes and conguraons, which ensure eecve treatment and max-
imum comfort. Refer to Compression Garment IFU for further informaon.
4 Chamber Garment (for use with SC-2004-OC or SC-2004FC-OC)
8 Chamber Garment (for use with SC-2008-OC)

FRONT PANEL—SC-2008-OC
Key Funcons
(Note: SC-2008-OC and SC-2004-OC, SC-2004FC-OC same key funcons. No Auxiliary Air Supply Ports on the SC-2004-OC/SC-2004FC-PC)
LATCH CONNECTORS
Aach and detach the garment to the pump via the Receptor Ports (for Tubing Latch Connector
Bars), depicted by #4 in the illustraon above. A second garment may be aached to the Auxiliary
Air Supply Ports for bilateral use. (IMPORTANT: Keep the Blocker bars installed for single garment use).
TUBING
Responsible for delivering air to and from the pump and garment.
COMPRESSION GARMENT
Garment with 4 or 8 chambers, which works in conjuncon with the Sequenal Circulator to apply controlled,
sequenal pressure throughout its chambers.
1Power On/O Switch
2Pressure Knob
3Receptor Ports (for Tubing Latch Connector Bars)
4Air Supply Ports , #1 - 4
5Air Supply Ports , #5 - 8
6Auxiliary Air Supply Ports (for Bilateral Use, shown with Blocker Bars Installed)
7Photo of Blocker Bars (uninstalled)
8Tubing Latch Connector Bars (shown on the end of Tubing)
78
1 2
3
5
6
4

OPERATING INSTRUCTIONS
Unpacking Equipment
1. Open the shipping box and li the device up and out of the box.
(Maintain shipping box for future use. Equipped with a special fold-up handle for
ease of use).
2. Remove the protecve end caps from the sides of the device.
3. Remove the garment from the plasc bag and unroll both tubing secons.
Unfold the garment and spread it at.
Preparing for Treatment
4. Place the device on a at and sturdy surface in close proximity to the paent.
5. Plug the power cord into a safe electrical outlet. A grounded outlet is not required.
6. Locate the Latch Connector Bars, numbered 1-4, at the end of the garment tubing.
7. Hold in one hand with numbers facing upward. Squeeze the sides of the Latch
Connector Bar and insert receptor ports into the corresponding numbered air supply
ports. There shall be an audible ’click’ once fully engaged.
8. If two (2) garments are being used simultaneously, remove the Blocker Bars, and
aach the Latch Connector Bars to the corresponding numbered auxiliary ports.
Axing the Compression Garments
Cauon: Do not wear garments directly on bare skin. Always wear light clothing,
light bandages, clean hosiery or stockinees underneath garments for hygienic pur-
poses and to prevent skin irritaon. Clothing must be free of zippers, buons and
other items that could rub and chafe the skin or damage the compression garment.
9. Leg Garments - Carefully unzip the garment fully without separang the zipper at the
end. Place foot at boom end of garment and use garment straps to guide garment
onto the leg. Once garment is fully in place, pull zipper up to secure garment around
the leg.
10. Arm Garments - Slide arm through the internal cavity of the garment.

Powering On the Sequenal Circulator
11. Paent shall be seated in a reclined posion, legs elevated within easy reach of the
Sequenal Circulator.
12. Press the “Power On/O” buon to turn the pump on.
13. Within several seconds, the pump shall begin producing air pressure. The air pressure
may be set in the same posion as the previous treatment. Factory default pressure is
50 mmHg in the chamber #1, decreasing incrementally as it moves distally to proximally
between zones.
Seng the Air Pressure on the Sequenal Circulator
14. Turn Pressure Knob to the prescribed seng.
15. The Pressure Knob determines the pressure in the distal chamber. Once set, the
Sequenal Circulator shall automacally set the subsequent pressure zones within the
garment, by incrementally decreasing each zone as the air pressure moves distally to
proximally.
16. Treatment me shall be determined by physician. Adhere to physician’s instrucon on
me alloed for each treatment.
Powering O the Sequenal Circulator
17. Upon compleon of treatment, press the “Power On/O” buon to turn o the pump.
The pump shall stop running at this me. Please note you must wait unl the light goes
out before removing your garment.
18. Prior to removing the garment, squeeze the sides of the Latch Connector Bars and
detach from pump by pulling outward away from pump. This will fully detach the
garment from the pump.
19. Depress the garment to help evacuate any remaining air. Once the garment becomes
loose enough to remove, unzip the garment and remove.
20. Repeat removal procedure for any addional garments being used.

CAUTION: In case of power failure, the Sequenal Circulator shall automacally power
o. The pump does not have a baery backup nor mer memory. Once power is re-
stored, the Sequenal Circulator will need to be powered on in order to resume treat-
ment. User must keep apprised of alloed treatment me.
GENERAL GUIDELINES FOR TREATMENT
Physician must prescribe sengs for use with this device. The general guidelines below
are for informaonal purposes only and should not replace sengs provided by
physician. 60mmHg is an eecve seng for many paents. Physician must provide
paent’s sengs.
The presence of broc ssue may require a pressure of 80mmHg in order to soen the
broc ssue and achieve reducon. Once ssue soens, compression may be reduced
to 60mmHg, if determined by physician
Paents with a history of Congesve Heart Failure (CHF), which is controlled by
medicaon, should never be in a at posion while using the Sequenal Circulator. These
paents should be in a reclined posion with their legs elevated during treatment. It is
suggested that treatment regimens be divided into two daily 30-minute treatments.
Paents with a history of Deep Vein Thrombosis (DVT), with or without a lter, may
require less compression pressure, 40mmHG is generally tolerable but must be
prescribed by a physician. Paents with a lter may need to divide treatment into two
daily 30-minute sessions. It is suggested that the provider obtain a Negave Doppler
Study from the physician for their records.
MAINTENANCE AND STORAGE
Exterior Pump Case Cleaning instrucons:
1. Clean the exterior case and tubing with a damp (not wet) cloth using mild soap and
water soluon once per month
WARNING!
 Only an authorized technician may open the pump
 Before cleaning, unplug power cord from electrical outlet
GARMENT CLEANING/DISINFECTING INSTRUCTIONS:
Disconnect garment from device.
2. Open garment to expose all sides either by separang Velcro type hook and loop or
by unzipping (depending on type of garment).
WARNING!
 Do not allow liquids to enter pump, as this can present an electrical hazard
 Always allow the pump to dry before using
 Do not use bleach on the pump
3.Cleaning soluon should consist of 1/3 cup of laundry detergent per 1 gallon of
warm tap water. Use either a large sink or plasc tub able to hold enough soluon
(depending on size and quanty of garments) to completely submerge the garment
leaving the latch connector bars out of the water.

Garment Cleaning and Disinfecng—connued from previous page
4. Garment should be soaked for 30 minutes with mild agitaon every 5 to 10 minutes while
keeping it below water surface.
5. Thoroughly rinse garment with warm tap water and allow to air dry.
 WARNING! Never allow the Latch Connectors to be submerged into the water. If water
enters the inside of the garment, damage may occur to the device.
6. Harder to remove soil on surface of garment may require addional washing by hand with a
clean towel while submerged. Avoid using any abrasive materials such as scrubbing pads or
chemicals that could cause damage to the exterior surface of garment.
7. Re-Submerge garment for 30 minutes (with excepon of tubing connectors) in soluon con-
sisng of 1 cup of bleach per 1 gallon of warm tap water, again agitang garment every 5 to
10 minutes while keeping garment below water surface. Rinse garment thoroughly with
warm tap water and allow to air dry. This completes the disinfecng step.
 WARNING! DO NOT place garment in washing machine.
 WARNING! DO NOT use the tubing or valves as “handles” for carrying, handing or
storing garment.
TROUBLESHOOTING
If the correcve acon does not resolve the problem, please call Bio Compression Systems, Inc., at
1-800-888-0908. Serial number is required when calling for service.
Symptom Possible Cause Correcve Acon
The device is not working.
No electricity Check the electrical wall outlet to be sure that
the pump is plugged into the outlet correctly.
Check the circuit breaker to be sure there is
power to the outlet.
Power cord Unplug the power cord and look for any
damage or defects.
One garment inates but the
second one does not.
The second garment is not
receiving air.
Check the garment hoses for adequate con-
necon to the device, kinks, punctures, twists
and /or folds.
The device is making strange
and/or loud noises.
Device is on a uneven or unsta-
ble surface
Move to a more stable surface.
An internal problem Contact Bio Compression Systems, Inc., for
repair.
Regardless of the pressure
seng the garments are
applying a very low pressure.
Defecve Garment Check the garment for adequate connecon
to the device, leaks, kinks, punctures, twists
and /or folds.
An internal problem Contact Bio Compression Systems, Inc., for
repair.

REPAIR SERVICE INFORMATION
Technical Support—please call for all service repairs. Model and Serial numbers shall be
required for all service inquiries.
CAUTION: Tampering with or dismantling the Sequenal Circulator in any way shall void
the warranty on the device.
Warranty repairs or adjustments shall be performed in a mely manner with minimal
inconvenience. For this reason, it is important that you obtain a “Return Material
Authorizaon” Number (RMA #) when calling Customer Service.
WARRANTY INFORMATION
You can feel condent that your product is backed by the best warranty in the industry,
covering any and all malfuncons (including parts and labor) resulng from component
and/or manufacturing defects.
Compression Pump = 3 years from date of purchase / invoice
Sleeves/Garments = 1 year from date of purchase / invoice
Serial Number:
Date Purchased:
Local Representave/Dealer:
Phone Number:
DISPOSAL OF DEVICE
Medical equipment and devices should be disposed of in proper containers that meet
Environmental Protecon Agency standards. Check with your local, regional and naonal laws
and regulaons for specic requirements.

4 CHAMBER GARMENT SPECIFICATIONS (for use with SC-2004-OC & SC-2004FC-OC)
PRODUCT APPLICATION SIZE SIDE
GS-3035-SArm Small
GS-3035-MArm Medium
GS-3035-LArm Large
GS-3035-SH/S Arm & Shoulder Small
GS-3035-SH/M Arm & Shoulder Medium
GS-3035-SH/L Arm & Shoulder Large
GA-3035-SArm Small Adjustable
GA-3035-MArm Medium Adjustable
GA-3035-LArm Large Adjustable
GV-3000 Vest
GS-3045-HHalf Leg Half
GS-3045-SFull Leg Small
GS-3045-MFull Leg Medium
GS-3045-LFull Leg Large
GN-3045-SFull Leg Small Narrow
GN-3045-MFull Leg Medium Narrow
GN-3045-LFull Leg Large Narrow
GW-3045-HHalf Leg Half Wide
GW-3045-SFull Leg Small Wide
GW-3045-MFull Leg Medium Wide
GW-3045-LFull Leg Large Wide
GXW-3045 Full Leg Extra Wide
GA-3045-HFull Leg Half Adjustable
GA-3045-SFull Leg Small Adjustable
GA-3045-MFull Leg Medium Adjustable
GA-3045-LFull Leg Large Adjustable
GWA-3045-SFull Leg Small Wide Adjustable
GWA-3045-MFull Leg Medium Wide Adjustable
GWA-3045-LFull Leg Large Wide Adjustable
GXWA-3045 Full Leg Extra Wide Adjustable
CG-3035-CArm Custom Arm
CG-3045-CFull Leg Custom Leg

8 CHAMBER GARMENT SPECIFICATIONS - (for use with SC-2008-OC)
PRODUCT APPLICATION SIZE SIDE
G8-3035-SArm Small
G8-3035-MArm Medium
G8-3035-LArm Large
G8-3035-SH/S Arm & Shoulder Small
G8-3035-SH/M Arm & Shoulder Medium
G8-3035-SH/L Arm & Shoulder Large
GV-3010-S-RArm Elite Bio Vest Small Right
GV-3010-S-LArm Elite Bio Vest Small Le
GV-3010-M-RArm Elite Bio Vest Medium Right
GV-3010-M-LArm Elite Bio Vest Medium Le
GV-3010-L-RArm Elite Bio Vest Large Right
GV-3010-L-LArm Elite Bio Vest Large Le
GV-3000-S-1Vest & Arm Small Le or Right
GV-3000-M-1Vest & Arm Medium Le or Right
GV-3000-L-1Vest & Arm Large Le or Right
GV-3000-S-2Vest & Arms Small (2) Le or Right
GV-3000-M-2Vest & Arms Medium (2) Le or Right
GV-3000-L-2Vest & Arms Large (2) Le or Right
G8-3045-SFull Leg Small
G8-3045-MFull Leg Medium
G8-3045-LFull Leg Large
GW8-3045-SFull Leg Small Wide
GW8-3045-MFull Leg Medium Wide
GW8-3045-LFull Leg Large Wide
GXW8-3045 Full Leg Extra Wide
A8-3045-SFull Leg Small Adjustable
A8-3045-MFull Leg Medium Adjustable
A8-3045-LFull Leg Large Adjustable
GWA8-3045-SFull Leg Small Wide Adjustable
GWA8-3045-MFull Leg Medium Wide Adjustable
GWA8-3045-LFull Leg Large Wide Adjustable
GXWA8-3045 Full Leg Extra Wide Adjustable
GN8-3045-SFull Leg Small Narrow
GN8-3045-MFull Leg Medium Narrow
GN8-3045-LFull Leg Large Narrow
GBA-3045-M-2Bio Pants Custom
C8-3035-CArm Custom Arm
C8-3045-CFull Leg Custom Leg

GENERAL EQUIPMENT SPECIFICATIONS
ENVIRONMENTAL CONDITIONS
ELECTRICAL SPECIFICATIONS/EQUIPMENT CLASSIFICATION
The Sequenal Circulators, SC-2004-OC, SC-2004FC-OC and SC-2008-OC, interior components are
“double insulated” and do not require a “protecve ground.” The devices are equipped with
18 gauge, 2-wire, 10’ Power Cords, secured through the pump casings with a Heyco strain relief
brushing, as well as, an addional “hold-down” clamp for added safety.
 Class of protecon against electrical shock: CLASS II EQUIPMENT
 The degree of protecon against electric shock: APPLIED PART-TYPE B
 Mode: CONTINUOUS OPERATION WITH INTERMITTENT LOADING
 According degree of protecon against ingress of water: IXP0
SC-2004-OC SC-2008-OCSC-2004FC-OC
DIMENSIONS: 4.5” H x 11” W x 7” D 4.5” H x 11.75” W x 7.75” D4.5” H x 11” W x 7” D
WEIGHT: 5.5 lbs 5.5 lbs5.5 lbs
INFLATION: 72 Seconds 44 Seconds40 Seconds
DEFLATION: 18 Seconds 5.5 Seconds10 Seconds
CYCLE TIME: 18 Seconds / Chambers 5.5 Seconds / Chambers 10 Seconds
ELECTRICAL: 120 VAC, 60 Hz, 0.5 A (USA)
230 VAC,
120 VAC, 60 Hz, 0.5 A (USA)
230 VAC,
120 VAC, 60 Hz, 0.5 A (USA)
230 VAC,
APPLIED PART: TYPE B TYPE BTYPE B
PROTECTION AGAINST ELECTRICAL
SHOCK
CLASS II (USA)
CLASS IIa (EU)
CLASS II (USA)
CLASS IIa (EU)
CLASS II (USA)
CLASS IIa (EU)
OPERATION MODE: CONTINUOUS OPERATION CONTINUOUS OPERATIONCONTINUOUS OPERATION
PROTECTION MODE AGAINST WATER: IPX0 IPX0IPX0
FOR OPERATION
AMBIENT TEMPERATURE: +50°F - +110°F (+10°C -+44°C)
RELATIVE HUMIDITY: 30% - 75%
ATMOSPHERIC PRESSURE: 700hPa to 1060hPa
FOR TRANSPORT AND STORAGE
ATMOSPHERIC PRESSURE: -20°F - + 110°F (-29°C- +44°C)
RELATIVE HUMIDITY: 30% - 75%
ATMOSPHERIC PRESSURE: 700hPa - 1060hPa

Guidance and Manufacturer’s Declaraon — Electromagnec Immunity
The SC-2004-OC/SC-2004FC-OC/SC-2008-OC are intended for use in the electromagnec environment specied below. The customer or the
user of the SC-2004-OC/SC-2004FC-OC/ C-2008-OC should assure that it is used in such an environment.
Immunity
test
IEC 60601 test
level Compliance level Electromagnec environment—guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 1000-4-3
3 Vrms
15 kHz to 80
MHz
3 V/m
80 MHz to 2.5
GHz
3 Vrms
3 V/m
Portable and mobile RF communicaons equipment should be used no closer to any
part of the model SC-2004-OC/SC-2004FC-OC/SC-2008-OC, than the recommended
separaon distance calculated from the equaon applicable to the frequency of the
transmier.
Recommended separaon distance
80 MHz to 800 MHz
800 MHz to 2.5 GHz
where P is the maximum output power rang of the transmier in was (W) accord-
ing to the transmier manufacturer and d is the recommended separaon distance
in meters (m).
Field strengths from xed RF transmiers, as determined by an electromagnec site
survey,a should be less than the compliance level in each frequency range.b
Interference may occur in the vicinity of equipment marked with the following sym-
bol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply to all situaons. Electromagnec propagaons is aected by absorpon and reecons from struc-
tures, objects and people.
a Field strengths from xed transmiers, such as base staons for radio (cellular/cordless) telephones and land mobile radios, amateur ra-
dio, AM and FM radio broadcast and TV broadcast cannot be predicted theorecally with accuracy. To assess the electromagnec environ-
ment due to xed RF
transmiers, an electromagnec site survey should be considered. if the measured eld strength in the locaon in which the model SC-
2004-OC/SC-2004FC-OC/SC-2008-OC is used exceeds the applicable RF compliance level above, the model SC-2004-OC/SC-2004FC-OC/SC-
2008-OC should be observed to verify normal operaon. If abnormal performance is observed, addional measures may be necessary,
such as re-orienng or relocang the model SC-2004-OC/SC-2004FC-OC/SC-2008-OC.
b Over the frequency range 150 kHZ to 80 MHz, eld strengths should be less than 3 V/m.
Model SC-2004-OC/SC-2004FC-OC/SC-2008-OC Electromagnec Emissions—Manufacturer’s Declaraon
The SC-2004-OC/SC-2004FC-OC/SC-2008-OC are intended for use in the electromagnec environment specied below. The customer or the
user of the SC-2004-OC/SC-2004FC-OC/SC-2008-OC should assure that it is used in such an environment.
Emissions test Compliance Electromagnec environment— guidance
RF emissions
CISPR 11
Group 1 The model SC-2004-OC/SC-2004FC-OC/SC-2008-OC uses RF energy only for its internal
funcons. Therefore, its RF emissions are very low and are not likely to cause any inter-
ference in nearby electronic equipment.
RF emissions
CISPR 11
Class B
The model SC-2004-OC/SC-2004FC-OC/SC-2008-OC is suitable for use in all establish-
ments, including domesc establishments and those directly connected to the public
low voltage power supply network that supplies building used for domesc purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage uctuaons / icker
emissions
IEC 61000-3-3
Not applicable

Recommended separaon distances between portable and mobile RF communicaons equipment
and the SC-2004-OC/SC-2004FC-OC/SC-2008-OC
The SC-2004-OC/SC-2004FC-OC/SC-2008-OC are intended for use in an electromagnec environment in which radiated RF disturbances are
controlled. The customer of user of the SC-2004-OC/SC-2004FC-OC/SC-2008-OC can help prevent electromagnec interference by maintain-
ing a minimum distance between portable and mobile RF communicaons equipment (transmiers) and the SC-2004-OC/SC-2004FC-OC/SC-
2008-OC as recommended below, according to the maximum output power of the communicaons equipment.
Rated maximum output power
of transmier
W
Separaon distance according to frequency of transmier
m
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
11.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmiers rated at a maximum output power not listed above, the recommended separaon distance d in meters (m) can be esmated
using the equaon applicable to the frequency of the transmier, where p is the maximum output power rang of the transmier in was
(W) according to the transmier manufacturer.
Note 1: At 80 MHz, the separaon distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situaons. Electromagnec propagaon is aected by absorpon and reecon from struc-
tures, objects and people.
Guidance and Manufacturer’s Declaraon—Electromagnec Immunity
The SC-2004-OC/SC-2004FC-OC/SC-2008-OC are intended for use in the electromagnec environment specied below. The customer or the
user of the SC-2004-OC/SC-2004FC-OC/SC-2008-OC should assure that it is used in such an environment.
Immunity test IEC 60601
test level Compliance level Electromagnec environment— guidance
Electrostac
discharge (ESD)
IEC 61000-4-2
± 2, 4, and6 kV contact
± 2, 4 and 8 kV air
± 2, 4, and6 kV contact
± 2, 4 and 8 kV air
Floors should be wood, concrete or
ceramic le. If oors are covered with
synthec material, the relave humidi-
ty should be at least 30%.
Electrostac
fast transient /
burst
IEC 61000-4-4
± 2 kV for power supply lines
± 1 kV for input / output lines
± 2 kV
Not applicable
Mains power quality should be that of a
typical home use locaon.
Surge
IEC 61000-4-5
± 0.5 and 1 kV line(s) to line(s)
± 2 kV line(s) to earth
± 0.5 and 1 kV dierenal mode
Not applicable, no ground wire
Mains power quality should be that of a
typical home use locaon.
Voltage dips,
short
interrupons and
voltage variaons
on power supply
input lines
IEC 61000-4-11
<5 % UT (>95% dip in UT) for 0.5 cycles
40 % UT (60% dip in UT) for 6 cycles
70 % UT (30% dip in UT) for 30 cycles
<5 % UT (>95% dip in UT) for 5 s
<5 % UT (>95% dip in UT) for 0.5
cycles
40 % UT (60% dip in UT) for 6 cycles
70 % UT (30% dip in UT) for 30 cycles
<5 % UT (>95% dip in UT) for 5 s
Mains power quality should be that of a
typical home use locaon. If the user
of the model SC-2004-OC/SC-2004FC-
OC/SC-2008-OC requires connued
operaon during mains power interrup-
ons, it is recommended that the mod-
el SC-2004-OC/SC-2004FC-OC/SC-2008-
OC be powered from an uninterrupble
power supply or a baery.
Power frequency
(50/60 Hz) mag-
nec eld
IEC 61000-4-8
3 A/m 3 A/m The power frequency magnec elds
should be at the levels found in a typi-
cal home use locaon.
NOTE: UT is the AC mains voltage prior to applicaon of the test level.