Keeler KSL-H User manual

SLIT LAMP
INSTRUCTIONS FOR USE
Digital IFU supplement
A world without vision loss
&

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KSL-H AND KSL-Z by KEELER
CONTENTS
1. INDICATIONS FOR USE ........................................................................................ 3
2. SAFETY................................................................................................................. 3
2.1 PHOTOTOXICITY ............................................................................................................................3
2.2 WARNINGS AND CAUTIONS..........................................................................................................4
2.3 CONTRAINDICATION.....................................................................................................................5
3. CLEANING AND DISINFECTION INSTRUCTIONS.................................................... 6
4. INSTALLATION OF DIGITAL UNIT .......................................................................... 6
4.1 KSL-H SERIES SLIT LAMP................................................................................................................9
4.2 KSL-Z SERIES SLIT LAMP................................................................................................................9
5. CONTROLS.......................................................................................................... 10
5.1 BACKGROUND ILLUMINATION ADJUSTMENT ..............................................................................10
5.2 EXPOSURE AND REVIEW BUTTONS..............................................................................................10
5.3 CAPTURE BUTTON.......................................................................................................................10
5.4 KEYBOARD SHORTCUTS ..............................................................................................................10
6. WARRANTY ........................................................................................................ 11
7. SPECIFICATIONS AND ELECTRICAL RATINGS...................................................... 11
7.1 ELECTROMAGNETIC EMISSIONS..................................................................................................11
7.2 ELECTROMAGNETIC IMMUNITY ..................................................................................................12
7.3 RECOMMENDED SAFE DISTANCES ..............................................................................................13
8. TECHNICAL SPECIFICATIONS.............................................................................. 14
9. DIGITAL ACCESSORIES/SPARES .......................................................................... 16
10. PACKAGING AND DISPOSAL INFORMATION....................................................... 17

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Consult instructions for use General warning sign
Date of manufacture Warning: Electricity
Manufacturer’s name and
address Warning: Floor level obstacle
Country of manufacture Warning: Non-ionizing
radiation
Waste Electrical and Electronic
Equipment (WEEE) recycling Warning: Optical radiation
This way up Warning: Hot surface
Keep dry Conformité Européene
Fragile Type B applied part
Do not use if package is
damaged Class II equipment
Temperature limit Atmospheric pressure
limitation
Authorised representative in
the European Community Humidity limitation
Use-by date Serial number
Catalogue number Medical device
Translation
The Keeler Slit Lamp Digital IFU is designed and built in conformity with Directive 93/42/EEC, Regulation (EU)
2017/745 and ISO 13485 Medical Devices Quality Management Systems.
Classification: CE: Class I
FDA: Class II
The information contained within this manual must not be reproduced in whole or part without the manufacturer’s
prior written approval. As part of our policy for continued product development we the manufacturer reserve the right
to make changes to specifications and other information contained in this document without prior notice.
This IFU is also available on the Keeler UK and Keeler USA websites.
Copyright © Keeler Limited 2021. Published in the UK 2021.

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KSL-H AND KSL-Z by KEELER
1. INDICATIONS FOR USE
This device is intended to be used only by suitably trained and authorised healthcare
professionals.
CAUTION: Federal Law restricts this device to sale by or on the order of a
physician or practitioner.
Intended use / purpose of instrument
The Keeler Slit Lamp facilitates an examination of the anterior segment, or frontal structures
and posterior segment, of the human eye, which includes the eyelid, sclera, conjunctiva, iris,
natural crystalline lens and cornea.The binocular slit-lamp provides stereoscopic magnified
view of the eye structures in detail, enabling anatomical diagnoses to be made for a variety of
eye conditions.
Brief description of the instrument
This Keeler Slit Lamp can either be mounted onto a custom table top supplied by Keeler or can
be mounted on a third parties table top (refraction unit) by suitably trained technicians.
The Keeler Slit Lamp consists of 5 assemblies; illumination tower; observation system; XYZ
translation base; chinrest assembly and a table top with power supply and accessory drawer.
The light intensity is controlled by a variable rheostat located on the XYZ translation base.
There are a number of selectable filters allowing the user to control the characteristics of the
examination light.
2. SAFETY
2.1 PHOTOTOXICITY
CAUTION: The light emitted from this instrument is potentially hazardous.
The longer the duration of exposure, the greater the risk of ocular
damage. Exposure to light from this instrument when operated at
maximum intensity will exceed the safety guideline after 171 seconds for
KSL-H and 81 seconds for KSL-Z.
While no acute optical radiation hazards have been identified for slit
lamps, we recommend keeping the intensity of the light reaching the
patient’s retina to the minimum possible for the respective diagnosis.
Children, people with aphakia and people suffering from eye conditions
are most at risk. An increased risk may also occur if the retina is exposed
to the same or a similar device with a visible light source within 24 hours.
This applies, in particular, if the retina has been photographed with a
flashbulb in advance.
Keeler Ltd shall on request, provide the user with a graph showing the
relative spectral output of the instrument.

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2.2 WARNINGS AND CAUTIONS
Please note that the proper and safe functioning of our instruments is only guaranteed if
both the instruments and their accessories are exclusively from Keeler Ltd. The use of other
accessories may result in increased electromagnetic emissions or reduced electromagnetic
immunity of the device and may lead to incorrect operation.
Observe the following precautions in order to ensure safe operation of the instrument For the
safety warning regarding the Keeler Slit Lamp please consult the Keeler Slit Lamp IFU.
WARNINGS
• Never use the instrument if visibly damaged and periodically inspect it for signs of damage
or misuse.
• Check your Keeler product for signs of transport / storage damage prior to use.
• Do not use in the presence of flammable gases / liquids, or in an oxygen rich environment.
• US Federal Law restricts this device to sale by or on the order of a physician or practitioner.
• This device is intended to be used only by suitably trained and authorised healthcare
professionals.
• This product should not be immersed in fluid.
• Repairs and modifications to the instrument must be made only by the specialized
technicians of the manufacturer’s Technical Service Centre or by personnel trained and
authorised by the manufacturer. The manufacturer declines any and all responsibility for
loss and/or damages resulting from unauthorised repairs; furthermore, any such actions
will invalidate the warranty.
• The power switch and mains plug are the means of isolating the device from the mains
supply - ensure both the power switch and mains plug are accessible at all times.
• Do not position the equipment so that is difficult to press the power switch or remove the
mains plug from the wall socket.
• Route power cords safely to eliminate risk of tripping or damage to user.
• As the Digital Camera Assembly is medical equipment, special precautions are needed
regarding EMC (electromagnetic compatibility)
• It is important that the Digital Camera Assembly is configured and installed/put into
service, in accordance with the instructions/guidance provided herein and is used only in
the configuration as supplied.
• Do not exceed maximum recommended exposure time.
• Should the instrument suffer shocks (for example, should it accidentally fall), and the optical
system or the illumination system are damaged it may be necessary to return the instrument
to the manufacturer for repair.

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KSL-H AND KSL-Z by KEELER
• Do not touch accessible connectors and the patient simultaneously.
• The owner of the instrument is responsible for training personnel in its correct use.
• Ensure the instrument or instrument table is placed on a level and stable surface.
• Use only genuine Keeler approved parts and accessories or device safety and performance
may be compromised.
• Refraction stand variants or adaptors should only be used in combination with EN/IEC
60601-1 and EN/IEC 60601-1-2 compliant power supplies and devices.
• Shut down after every use. In case the dust cover is used: risk of overheating.
• For indoor use only (protect from moisture).
• Electrical equipment can be affected by electromagnetic interference, for example
videostream may freeze for one minute or more. If this occurs whilst using this equipment,
switch the unit off and reposition. Essential performance is determined as continuous
videostream which cannot be interrupted for longer than one minute.
• Despite the testing of the Digital Camera Assembly that has been undertaken, normal
operation of the Digital Camera Assembly can be affected by other electrical/electronic
equipment and portable and mobile RF communications equipment.
• Keeler digital KSL is not intended to be used with wireless technology. Do not plug
a wireless dongle into USB port. It is advisable to disable wireless technology on the
computer to prevent unauthorised access to the camera.
• Keeler digital KSL cannot be used in the vicinity of sources known to cause electromagnetic
disturbance (magnetic resonance imaging, computed tomography, radio-frequency
identification, metal detectors, electronic article surveillance and other electromagnetic
security systems). Do not bring the Keeler digital Slit lamp into magnetic resonance
environment.
• The Digital Camera Assembly should not be used adjacent to or stacked with other
equipment. If adjacent or stacked use with other equipment is necessary, the Digital
Camera Assembly and the other equipment should be observed / monitored, to verify
normal operation in the configuration in which it will be used.
Before use, the Slit Lamp should be allowed to adjust to the ambient
room temperature for several hours. This is especially important when the
unit has been stored or transported in a cold environment; this can cause
severe condensation to develop on the optical elements.
2.3 CONTRAINDICATION
There is no restriction to patient population this device can be used with other than those
outlined in the contra-indications stated below.
Slit lamps can produce discomfort in some photophobic patients due to the high illumination.
Additionally patients must be co-operative and capable of sitting upright for the duration of
the examination, therefore the technique may not be suitable for patients who are unable to sit
upright for long periods of time or those with limited neck and back mobility.

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KSL-H AND KSL-Z by KEELER
3. CLEANING AND DISINFECTION INSTRUCTIONS
Before any cleaning of the instrument or the base unit, ensure the power
lead is disconnected.
Only manual non-immersion cleaning as described should be used for this instrument. Do not
autoclave or immerse in cleaning fluids. Always disconnect power supply from source before
cleaning.
1. Wipe the external surface with a clean absorbent, non-shedding cloth dampened with
de-ionised water / detergent solution (2% detergent by volume) or water / isopropyl
alcohol solution (70% IPA by volume). Avoid optical surfaces.
2. Ensure that excess solution does not enter the instrument. Use caution to ensure cloth is
not saturated with solution.
3. Surfaces must be carefully hand-dried using a clean non-shedding cloth.
4. Safely dispose of used cleaning materials.
4. INSTALLATION OF DIGITAL UNIT
For ‘Digital Ready’ variants of the Keeler Slit Lamp a Digital Camera Assembly (DCA) must be
purchased separately, contact Keeler or your local distributor for details.
Set up the Slit Lamp as directed in the Instructions For Use (IFU) EP59-70040 or EP59-70043,
contact your distributor if you are unable to locate a copy of these instructions.
1. Install the DCA carefully remove the eyepiece assembly from the magnification block by
unscrewing the securing knob at the same time as supporting the eyepieces. The
eyepieces assembly is a dovetail type fit to the magnification block.
Care must be taken to avoid getting any dirt or dust on any of the optical
components.
Securing knob

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KSL-H AND KSL-Z by KEELER
2. Fit the DCA to the rear of the magnification block and tighten the securing knob to hold
it in place.
3. Re-fit the eyepiece assembly to the rear of the DCA and secure it by tightening the
securing knob.
4. Rotate the swing arm to either side of the unit, and with a suitable Philips screwdriver
remove the cable channel cover plate.

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KSL-H AND KSL-Z by KEELER
5. Remove the cover to the USB hub on the Slit Lamp base by undoing the small Phillips
head screw and lifting off the cover.
6. Connect the shorter USB cable (3020-P-7107) to the socket on the underside of the DCA
and to the appropriate socket on the USB hub located on the Slit Lamp base. Ensure that
there is plenty of slack at the USB hub end to allow Slit Arm rotation.
7. Route the cable in the groove in the Slit Lamp arm and replace the cover plate.
8. Connect the longer USB cable for connection to the PC to the hub and replace the USB
hub cover plate, this secures the cables.
to camera
to PC

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KSL-H AND KSL-Z by KEELER
4.1 KSL-H SERIES SLIT LAMP
1. Clip the auxiliary diffuser and blue filter in place on the Slit Lamp tower upright posts,
above the level of the mirror. Align the slot to the flattened post section.
2. Fit the background illumination fibre optic cable, The short end to the top of the lamp
housing, the long end to the fibre optic swing arm adjacent to the mirror.
3. If CE compliant or FDA cleared imaging software has been installed, connect the PC USB
cable to the PC.
4.2 KSL-Z SERIES SLIT LAMP
1. No fitting of the background light is required as the Slit Lamp comes fully assembled.
long end
short end

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5. CONTROLS
5.1 BACKGROUND ILLUMINATION ADJUSTMENT
5.2 EXPOSURE AND REVIEW BUTTONS
Pressing these buttons provides adjustment of the camera exposure.
5.3 CAPTURE BUTTON
Press once to ‘freeze frame’.
Use image review buttons to select best frame.
Press again to capture selected frame.
5.4 KEYBOARD SHORTCUTS
Press Ctrl + Alt + Shift with function keys
F6 Right eye F9 Review freeze frame images forwards
F7 Left eye F10 Shorter exposure time
F8 Freeze frame / Trigger F10 Review freeze frame images
backwards
F9 Longer exposure time
KSL-H SERIES SLIT LAMP KSL-Z SERIES SLIT LAMP
Increase exposure time (milliseconds)
Review freeze frame images forwards
Decrease exposure time (milliseconds)
Review freeze frame images backwards

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6. WARRANTY
The Keeler H-Series Slit Lamps are guaranteed for three years against faulty workmanship
materials or factory assembly. Warranty is on a Return To Base (RTB) basis at the cost of the
customer and may be void if the Slit Lamp has not been regularly serviced.
The manufacturer’s warranty and terms and conditions are detailed on the Keeler UK website.
The mirror, main illumination lamp and general ‘wear and tear’ are excluded from our standard
warranty.
The manufacturer declines any and all responsibility and warranty
coverage should the instrument be tampered with in any manner or
should routine maintenance be omitted or performed in manners not in
accordance with these manufacturer’s instructions.
There are no user serviceable parts in this instrument. Any servicing or
repairs should only be carried out by Keeler Ltd. or by suitably trained and
authorised distributors. Service manuals will be available to authorised
Keeler service centres and Keeler trained service personnel.
7. SPECIFICATIONS AND ELECTRICAL RATINGS
The Keeler Slit Lamp is a medical electrical instrument.The instrument requires special care
concerning electromagnetic compatibility (EMC). This Section describes its suitability in terms
of electromagnetic compatibility of this instrument. When installing or using this instrument,
please read carefully and observe what is described here.
Portable or mobile-type radio frequency communication units may have an adverse effect on
this instrument, resulting in malfunctioning.
7.1 ELECTROMAGNETIC EMISSIONS
Guidance and manufacturer’s declaration – electromagnetic emissions
The Digital Camera Assembly is intended for use in the electromagnetic environment specified
below. The customer or user of the Digital Camera Assembly should ensure that it is used in
such an environment.
Emissions test Compliance Electromagnetic environment – guidance
RF emissions CISPR 11 Group 1 The Keeler Slit Lamp 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 The Digital Camera Assembly is suitable for use in a
professional healthcare facility environment. The Digital
Camera Assembly is not intended for use in home
environment.
Harmonic emissions
IEC 61000-3-2
Class B

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Emissions test Compliance Electromagnetic environment – guidance
Voltage fluctuations /
flicker emissions IEC
61000-3-3
Complies
7.2 ELECTROMAGNETIC IMMUNITY
Guidance and manufacturer’s declaration – electromagnetic immunity
The Digital Camera Assembly is intended for use in the electromagnetic environment specified
below. The customer or user of the Digital Camera Assembly should ensure that it is used in
such an environment
Immunity test IEC 60601 Test
level
Compliance
level
Electromagnetic
environment – guidance
Electrostatic
discharge (ESD).
IEC 61000-4-2
± 8 kV contact
± 15 kV air
± 8 kV contact
± 15 kV air
Floors should be wood, concrete
or ceramic tile. If floors are
covered with synthetic material,
the relative humidity should be at
least 30%.
Electrical fast
transient/burst. IEC
61000-4-4
± 2 kV for power
supply lines
± 1 kV for power
supply lines
N/A
N/A
Mains power quality should be
that of a typical professional
healthcare facility environment.
Surge.
IEC 61000-4-5
± 1 kV line(s) to
line(s)
± 2 kV line(s) for
input/output line(s)
N/A
N/A
Mains power quality should be
that of a typical professional
healthcare facility environment.
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines.
IEC 61000-4-11
UT= 0% 0.5 cycle
(0, 45, 90, 135, 180,
225, 270, 315°)
UT= 0%; 1 cycle
UT= 70%;
25/30 cycles (@ 0°)
UT= 0%;
250/300 cycle
UT= 0% 0.5 cycle
(0, 45, 90, 135, 180,
225, 270, 315°)
UT= 0%; 1 cycle
UT= 70%;
25/30 cycles (@ 0°)
UT= 0%;
250/300 cycle
Mains power quality should be
that of a typical professional
healthcare facility environment.
If the user of the Digital Camera
Assembly requires continued
operations during power mains
interruptions, it is recommended
that the Digital Camera
Assembly be powered from an
uninterruptible power supply.
Power frequency
(50/60 Hz)
magnetic field. IEC
61000-4-8
30 A/m 30 A/m Power frequency magnetic fields
should be at a level characteristic
of a typical location in a typical
professional healthcare facility
environment.
Note: UTis the a. c. mains voltage prior to application of the test level.

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Immunity
test
IEC 60601
Test level
Compliance
level
Electromagnetic environment
– guidance
Portable and mobile RF communications equipment
should be used no closer to any part of the Digital
Camera Assembly, including cables, than the
recommended separation distances calculated from
the equation applicable to the frequency of the
transmitter.
Recommended separation distance
Conducted
RF IEC
61000-4-6
6 Vrms 150kHz
to 80MHz
6 V d = 1.2 √ p
Radiated
RF IEC
61000-4-3
10 V/m 80MHz
to 2.7GHz
10 V/m d = 1.2 √ p 80MHz to 800 MHz
d = 2.3 √ p 800MHz to 2.7GHz
Where p is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in metres (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site survey¹,
should be less than the compliance level in each
frequency range.²
Interference may occur in the vicinity of
equipment marked with this symbol.
Note: At 80MHz and 800MHz, the higher frequency range applies. These guide lines may not apply in all situations.
Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
1 Field strengths from fixed transmitters, such as base stations ( cellular / cordless) telephones and land mobile
radios, amateur radio,AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with
accuracy.To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey
should be considered. If the measured field strength in the location in which the Keeler Slit Lamp is used exceeds
the applicable RF compliance level above, the Keeler Slit Lamp should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such as re-orientating or relocating the
Keeler Slit Lamp.
2 Over the frequency range 150kHz to 80 MHz, field strengths should be less than 10 V/m.
7.3 RECOMMENDED SAFE DISTANCES
Recommended separation distances between portable and mobile RF communications
equipment and the Digital Camera Assembly
The Digital Camera Assembly is intended for the use in an electromagnetic environment in
which radiated RF disturbances are controlled.The customer or the user of the Digital Camera
Assembly can help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and the Digital

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Camera Assembly as recommended below, according to the maximum output power of the
communications equipment.
Rated maximum output
power of transmitter (W)
Separation distance according to frequency of
transmitter (m)
150 kHz to 80MHz
d = 1.2√ p
80MHz to 800MHz
d = 1.2√ p
800MHz to 2.7GHz
d = 2.3√ p
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended
separation distance in metres (m) can be determined 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: At 80MHz and 800MHz, the separation distance for the higher frequency applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
8. TECHNICAL SPECIFICATIONS
Digital System Camera
Camera Resolution 2048 x 1536
Pixel Class: 3 MPixel
Sensor size: 1/1.8"
Sensor Technology: CMOS COLOR
PC Specification PC compliant with Electrical Safety (Medical) EN/IEC 60601-1
CPU: i5, 8/256GB SSD
Memory: 8GB RAM or higher
2 USB slots must be available, USB port: 3.0 or higher which will
provide power to the camera (5V and up to 1A) and receive the
video data.
Hard disk speed 5200 rpm or higher
Operating system: Microsoft Windows 10 Pro
Windows 10 Pro
Recommended screen resolution: 1920 x 1200 pixels
Software requirements CE compliant or FDA cleared camera imaging software

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Weight, packed (approx.)
Digital Slit Lamp complete 20.0Kg, 75 x 54 x 45cm W x D x H
Protection against ingress IPxO
Class II ME equipment
Insulation between mains parts and the functional earth provide at least two means of protection.
Power Supply
Power supply unit Switch mode, (100V-240V input) +/- 10% multi plug compliant to EN/
IEC 60601-1 EN/IEC 61000-6-2, EN/IEC 61000-6-3
Fuse T2.5AH, 250V
Power supply output 12V DC: 2.5 amps must be EN/IEC 60601 compliant
Complies with Electrical Safety (Medical) EN/IEC 60601-1
Electromagnetic compatibility EN/IEC 60601-1-2
Ophthalmic instruments - Fundamental requirements and test methods
ISO 15004-1
Ophthalmic instruments - Optical radiation hazard ISO 15004-2
Fuse ratings and quantity
2.5 amp anti-surge
Fuse current 2.5A
Voltage rating V AC 250V
Breaking capacity 1500Amps
Blow characteristic: Time Delay
If the Digital camera Assembly is used with power supplies or cables other than those supplied,
this may result in increased emissions or decreased immunity of the Digital Camera Assembly in
relation to EMC performance.
It should be noted that neither the power supply nor the cables provided with the Digital
Camera Assembly should be used on other equipment. To do so may result in increased
emissions or decreased immunity of the other equipment in relation to EMC performance.
Environmental Conditions:
USE
35°C
10°C
90%
30%
1060 hPa
800 hPa
Shock (without packing) 10 g, duration 6 ms

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USE
STORAGE CONDITIONS
*50°C
-10°C
95%
10%
1060 hPa
700 hPa
TRANSPORT CONDITIONS
*50°C
-40°C
95%
10%
1060 hPa
500 hPa
Vibration, sinusoidal 10 Hz to 500 Hz: 0.5g
Shock 30 g, duration 6 ms
Bump 10 g, duration 6 ms
*This instrument does not meet the temperature requirements of ISO 15004-1 for storage and transportation. Do
not store or transport this instrument in conditions where the temperature may rise above 50 °C.
9. DIGITAL ACCESSORIES/SPARES
Item Part Number Description
Kapture Imaging Software Licence 3020-P-7036 Software is on a USB stick
Keeler Connect Software Licence 3020-P-7112 USB Key
Large P Table (1120mm x 590mm) 3020-P-7138 For Digital Ready KSL’s only
Large Rectangle Table
(1000mm x 400mm)
3020-P-7128
Table Leg – Offset 3020-P-7085 For use with large table options.
USB Cable camera to hub 3020-P-7107
USB cable hub to PC 3020-P-7029
External illuminator, H-series 3020-P-5039
Auxiliary diffuser, H-series 3020-P-7034
Auxiliary blue filter, H-series 3020-P-7035

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10. PACKAGING AND DISPOSAL INFORMATION
Disposal of old electrical and electronic equipment
This symbol on the product or on its packaging and instructions indicates
that this product shall not be treated as household waste.
To reduce the environmental impact of WEEE (Waste Electrical Electronic
Equipment) and minimise the volume of WEEE entering landfills we
encourage at product end of life that this equipment is recycled and reused.
If you need more information on the collection reuse and recycling then please
contact B2B Compliance on 01691 676124 ([phone]). (UK only).
Any serious incident that has occurred in relation to the device must be reported to
the manufacturer and the competent authority of your Member State.

A world without vision loss
Contact
Manufacturer
Keeler Limited
Clewer Hill Road
Windsor
Berkshire
SL4 4AA UK
Freephone 0800 521251
Tel [phone]
Fax[phone]
EP59-70041 Issue 12 Date of Issue 12/05/2021
USA Sales Office
Keeler USA
3222 Phoenixville Pike
Building #50
Malvern, PA 19355 USA
Toll Free 1 800 523 5620
Tel [phone]
Fax [phone]
India Office
Keeler India
Halma India Pvt. Ltd.
Plot No. A0147, Road No. 24
Wagle Industrial Estate
Thane West – 400604, Maharashtra
INDIA
Tel [phone]
China Office
Halma China Group
名称：沃迈（上海）机电有限
公司
地址：上海市闵行区金都路1165弄
123号23幢一号厂房三层B座
电话：[phone]
Visiometrics, S. L., Vinyals, 131
08221 Terrassa, Spain