MediCapture MTS156 User manual

MTS156
Monitor with Touch Screen
Instructions for Use
English
MTS156-IFU01-EN-230809-MC
Version 1.0
For more translations (available in pdf), please visit www.medicapture.com/support

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Precautions for Use
Warning
Indicates a potentially hazardous situation
or improper use that could result in serious
personal injuries or death.
NOTE: Background color: Yellow
Triangular band: Black
Symbol: Black
This image indicates the manufacturer
and appears next to the manufacturer’s
name and address.
Medical Device
Caution
Indicates a potentially hazardous situation or
improper use which, if not avoided, may result
in minor or moderate injury and/or appreciable
material, nancial and environmental damage.
This symbol informs the user that these
Instruction for Use and translated copies can be
downloaded from the MediCapture website at:
www.medicapture.com/support
Symbols on the product (Not all symbols are printed in all regions)
Symbols in the manual
Before attempting to set up the product,
carefully read through the Instructions for Use. REF Description of device (Catalog number)
This symbol indicates the manufacturer
and appears next to the manufacturer’s
name and address.
Serial Number
2023-05-29
This symbol indicates date of
manufacturing. It can also show
the country of origin.
This symbol indicates compliance with the
Waste Electrical and Electronic Equipment
Directive (WEEE Directive)
The product contains waste from electrical
and electronic equipment and should be
separately collected and not disposed of
as unsorted municipal waste.
Medical Device
Conformité Européenne
(European Conformity) Input DC 5V 3A
Power Information
This symbol indicates MediCapture´s
European Representative.
IP20
Ingress protection. Protection against
penetration of objects and liquids
Unique Device Identier Temperature limit for transport and storage
UKCA marking (UK Conformity Assessed.
Product conforms to the requirements of the
UK MDR 2002 for Class 1 devices)
Humidity limitation for transport and storage
Representative for Switzerland Atmospheric pressure limit for transport
and storage

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WARNING
Do not modify this equipment without authorization of the manufacturer.
To reduce the risk of re or shock hazard, do not expose this equipment to rain or moisture, this device is designed for
indoor use only.
Note:
To the user and/or patient: Any serious incident related to the product shall be reported to the manufacturer and to the
competent authority of the Member State where the user/patient is established.
CAUTION
To reduce the risk of re or shock hazard and annoying interference, use the recommended accessories only.
Do not use the device display for diagnosis or evaluation purposes.
Restrictions of use:
- Do not use this monitor for direct diagnostic purposes.
- Do not use this monitor for radiological images and not for digital mammography.
- Do not use this monitor for life supporting systems.
Never touch a patient and this touchscreen at the same time.
It is important to observe your obligations as the operator of this medical device to ensure its safe operation with no risk
of danger to patients, users or third parties.
Patients are not intended to be operators.
After a strong electrical disturbance, like lightning or a strong electrostatic discharge, the output signal of the host device
may shake, change in color, or turn black. If you see these symptoms, restart the device by turning off the power, waiting
a few seconds, and then turning on the power.
Disposal Method: Use your local regulations for proper disposal.

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(CANADA ONLY)
Note régionale pour le Canada
Précautions d’utilisation
AVERTISSEMENT
Indique une situation potentiellement
dangereuse ou une utilisation incorrecte
pouvant causer des blessures graves ou
la mort.
NOTE Couleur de fond : jaune
Contour du triangle : noir
Symbole : noir
Cette image désigne le fabricant ; elle apparaît
à côté du nom et de l’adresse du fabricant.
Dispositif médical
(Medical device)
ATTENTION
Indique une situation potentiellement
dangereuse ou une utilisation incorrecte
pouvant, si elle n’est pas évitée, occasionner
des blessures légères à modérées et/ou
d’importants dommages matériels, nanciers
et environnementaux.
Ce symbole informe l’utilisateur que ce mode
d’emploi et des copies traduites peuvent être
téléchargés sur le site Web de MediCapture
à l’adresse suivante
www.medicapture/support
Symboles utilisés sur le produit (Tous les symboles ne sont pas imprimés dans toutes les régions.)
Symboles utilisés dans le manuel
Avant d’installer le produit, lire attentivement
le mode d’emploi. REF Description de l’appareil (numéro de catalogue)
Cette image désigne le fabricant ; elle apparaît
à côté du nom et de l’adresse du fabricant.
Numéro de série
2023-05-29
Ce symbole indique la date de
fabrication. Il peut porter le pays
de fabrication sous la forme
d’une abréviation ISO.
Cette icône représente la conformité avec
la directive sur les déchets d’équipements
électriques et électroniques (directive
WEEE). Le produit contient des déchets
d’équipements électriques et électroniques,
et doit être collecté séparément et non
éliminé comme un déchet municipal non trié.
Dispositif médical
(Medical device)
Conformité Européenne
(European Conformity)
Informations sur l’alimentation électrique
Ce symbole indique le représentant
européen de MediCapture.
IP20
Ingress protection. Protection contre les
intrusions d’objets et de liquides.
Identicateur unique du dispositif.
(Unique Device Identier)
Limite de température pour le transport
et le stockageå
Marquage UKCA (UK Conformity Assessed.
Le produit est conforme aux exigences du
UK MDR 2002 pour les appareils de classe 1)
Limitation de l’humidité pour le transport
et le stockage
Représentant pour la Suisse Limite de pression atmosphérique pour le
transport et le stockage
Input DC 5V 3A

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MISE EN GARDE
Ne pas modier cet équipment sans autorisation expresse du fabricant
An de réduire les risques d’incendie ou d’électrocution, n’exposez pas cet équipement à la pluie ou à l’humidité. Cet équipment est exclusivement
destiné à un usage intérieur.
Avis :
A l’attention de l’utilisateur et/ou du patient : Tout incident grave lié au produit doit être signalé au fabricant et à l’autorité compétente de l’État
membre où l’utilisateur/patient est établi.
ATTENTION
An de réduire les risques d’incendie ou de choc électrique et les interférences nuisibles, utilisez uniquement les accessoires recommandés.
Ne pas utiliser l’afchage de l’appareil à des ns d’évaluation ou de diagnostic.
Restrictions d’utilisation :
- N’utilisez pas ce moniteur à des ns de diagnostic direct.
- N’utilisez pas ce moniteur pour des images radiologiques et pas pour la mammographie numérique.
- N’utilisez pas ce moniteur pour les systèmes de survie.
Ne touchez jamais un patient et cet écran tactile en même temps.
L’exploitant doit utiliser cet équipement conformément aux recommandations du manuel utilisateur an d’assurer un fonctionnement sans risque ni
danger pour le patient, l’utilisateur ou tout autre partie.
Les patients ne sont pas destinés à être des opérateurs.
Après une perturbation électrique forte, comme la foudre ou une forte décharge électrostatique, le signal vidéo de sortie de l’appareil hôte peut
vaciller, changer de couleur ou devenir noir. Si ces symptômes apparaissent, redémarrer l’équipement en l’éteignant puis en le redémarrant après
avoir attendu quelques secondes.
Mise au rebut : Pour la mise au rebut du produit, respecter les règlements et les lois appropriés valides dans votre pays.
(CANADA ONLY)
Note régionale pour le Canada

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Table of Contents
Technical Support..............................................................................................................................................................6
Residual Risks...................................................................................................................................................................7
Important Safety Instructions to avoid residual risks. ...................................................................................................7
Data Protection..................................................................................................................................................................8
Intended Use:....................................................................................................................................................................8
General Functional Description: . .................................................................................................................................8
First installation / General preparations for safe operation and performance:..............................................................8
Checks before you operate the device: .......................................................................................................................9
Compatibility to Other Devices ..........................................................................................................................................9
Front Panel - Touchscreen ................................................................................................................................................9
Back Panel - Connections ...............................................................................................................................................10
Backside, side connections and buttons.....................................................................................................................10
Display Brightness......................................................................................................................................................10
Menu Settings.............................................................................................................................................................10
Backside, bottom connections....................................................................................................................................10
Back Panel - VESA Mount ..............................................................................................................................................11
Troubleshooting...............................................................................................................................................................11
Appendix A: MTS156 Specications................................................................................................................................12
Compliance / Certication / Classication...................................................................................................................13
Appendix B: MediCapture Limited Warranty....................................................................................................................14
Technical Support
For technical support and other questions, please visit medicapture.com or
call 888-922-7887 (toll free from within the USA) or [phone] (from outside the USA).
MediCapture®Inc. EC REP: MediCapture Europe B.V UKRP: United Kingdom
2250 Hickory Road, Suite 200 Stationsplein 5 Responsible Person
Plymouth Meeting, PA 19462 6131 AT Sittard Advena Ltd
USA The Netherlands Pure Ofces, Plato Close
[phone] Tachbrook Park
Warwick, CV34 6WE UK
CH REP: Jan Möstel
Robert-Seidel-Hof 70
, CH-8048 Zürich
Contact: www.medicapture.com/contact.php

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Residual Risks
Important Safety Instructions to avoid residual risks.
1. Read all of these instructions and Instructions for Use of the host device.
2. Keep these instructions.
3. Heed all warnings in these instructions.
4. Follow all of these instructions.
5. Do not misuse this apparatus.
6. Make sure that your video source is directly connected to the main monitor via primary safety wiring.
7. Clean the device regularly with a soft cloth moistened with ethanol 75%. Follow the disinfectant
manufacturer’s instructions!
▪ Before disinfection, the device must be cleaned to remove debris. Removal of debris can be accomplished by using a
dry, clean cloth.
• Disinfectant/sterilant: U.S. Environmental Protection Agency (EPA) approved
▪ Ethyl Alcohol, 75%
▪ Pour approximately 5ml of ethyl alcohol on a sterile cotton swab.
▪ Swipe the surface area of the device being careful not to come in contact with any of electrical connections on the back.
IMPORTANT! Make sure that no humidity enters the device. Do not use any cleaning agents, scouring agents
or solvents on this device.
8. Do not install near any heat source such as radiators, heat registers, stoves or other apparatus that produces heat.
9. Only use attachments/accessories specied by the manufacturer.
10. This device is only use in mounting status as a FIX type equipment. According to US deviation in 60601-1, FIX type equipment
shall be Class I type to comply with NEC requirement.
All FIXED medical electrical (ME) EQUIPMENT and PERMANENTLY INSTALLED medical electrical (ME) EQUIPMENT shall
be CLASS I medical electrical (ME) EQUIPMENT.
11. When using the VESA mounting option, make sure that the screws are the correct length. Screws that are too long may
damage the product, and screws that are too short may compromise stability.
See chapter Back Panel – VESA Mount.
12. Ensure that the mount is installed by qualied personnel and follow the instructions for the VESA mount (not supplied by
MediCapture).
The ACCOMPANYING DOCUMENTS shall contain instructions on attachment of structures to a oor, wall, ceiling, etc.
making adequate allowances for quality of the materials used to make the connection and shall list the required
materials. Additionally, there shall be advice on checking the adequacy of the surface of the structure to which the
parts will be attached.
13. Unplug this apparatus during lightning storms or when unused for long periods of time
Disconnection Method: Disconnect the USB cable.
14. Do not place vessels containing water or other liquids (such as vases, etc.) on top of the apparatus. Do not splash water on
top of the apparatus.
15. Refer all servicing to qualied service personnel. Servicing is required when the apparatus has been damaged in any way,
such as when a plug has been damaged, liquid has been spilled on the apparatus, objects have fallen into the apparatus, and
the apparatus has been exposed to rain or moisture, or does not operate normally, or has been dropped.
16. In case of breakdown, Service Equipment is performed by qualied personnel only, where qualied personnel refers to the
person with proper education or training assigned by the hospital, medical institution or authorized distributor.
17. This device does not have any serviceable parts. Repairs are carried out exclusively in MediCapture
service centers.
18. This device shall be used with a Class 1 type host device.
19. This equipment complies with the IEC 60601 safety standard only when connected to equipment that complies with the
IEC 60601-1 standard or applicable ISO or IEC standards. Anyone who connects equipment to the signal input is conguring
a medical system and is therefore responsible that the system complies with the requirements of medical system standard
IEC 60601-1. Equipment not complying with UL/EN/IEC 60601-1 shall be kept outside the patient environment, as dened on
the systems standard.

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Data Protection
This device does not come into contact with patient related data or protected health information (PHI) and does not store any data.
Intended Use:
This device is intended as user interface (human-machine interface) for various medical devices. It is not intended for
diagnostic purposes.
The intended patient population are not specied for this device.
User Qualication
This product is intended only for use in professional healthcare environments and by healthcare professionals who have
a corresponding specialized qualication.
Contra Indications and side effects:
Contraindications directly related to the product are presently unknown. On the basis of the patient‘s general condition the
doctor in charge must decide whether the planned use is possible or not. For further notes and instructions please refer to
the latest medical literature.
General Functional Description: .
This touchscreen monitor is used for external operation of devices with a graphical user interface. Power is supplied via USB of
the host device or via external DC power supply. Supply of graphic information (video signal) is via HDMI, DVI or USB-type C.
The start-up takes place automatically as soon as the supply voltage and the video signal are present and recognized.
First installation / General preparations for safe operation and performance:
1. Mounting:
Mount the MTS according to your preferences using the connection option on the back (VESA 75
or VESA 100 standard) for a stable connection.
MediCapture recommends an installation in a location where air can provide proper cooling. It is
not recommended to stack this MTS with converters or other warm devices.
2. Graphical information:
Connect the graphical interface connection / video connection to the HDMI port. (HDMI or DVI on
host device).
USB-type C video connections from the host device may also be able to transmit graphical information.
3. Connect a USB cable with the USB port (Type C) of MTS156 to a USB-A port (Type A) of the host
device, for example an MVR recorder. MTS156 requires about 5V, 1.5 A power from the USB port
of the host device. To provide MTS156 with sufcient power, it is recommended to connect it to
the USB3.0 host port (blue color) or external power supply.
4. Turn on your host device.
5. Check the image display and the touchscreen function. Multi-touch up to 10 ngers is supported.

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Checks before you operate the device:
The operation of this device does not require special maintenance, calibration or the use of consumable components. The hygiene
ofcer of the operator should follow its own disinfection plan for cleaning devices.
Start:
Simply switch on the host device. The monitor starts automatically as soon as both power and video signal are present.
Switch-off method:
Turn-off the host device.
Alternative method:
Press and hold MENU key for 3 seconds.
Standby Mode:
MTS156 automatically enters standby mode 65 seconds after video input signal is interrupted (no video input signal).
Note: If you want to turn off (terminate) the MTS monitor permanently, please disconnect the USB cable from the host device.
Compatibility to Other Devices
MTS156 is compatible with MediCapture MVR and MVR Lite medical video recorders.
MTS156 shall be operated by Class I type medical grade host devices only.
The compatibility requirements for medical video sources in terms of video signal and power supply can be found in “Appendix A:
MTS156 Specications” in this document.
Front Panel - Touchscreen
The monitor front offers a multi-touch function, e.g. for magnifying objects with two ngers.

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Back - Connections
Backside, side connections and buttons
Display Brightness
Press the “+” ① and “-” ②keys directly to change the brightness of the display. The setting is displayed in the menu.
Please note: It may be helpful to reduce the brightness to match the power consumption of the MTS
to the performance of the USB port of the host device.
Menu Settings
Settings in the menu of the monitor are intended for technical personnel. The menu navigation is intuitive.
The menu disappears automatically after 5 seconds of inactivity.
1. Press the Menu key ③ to open the menu.
2. The “+” ① and “-” ②keys move the cursor to the desired setting.
3. Pressing the Menu key ③again activates the setting of a parameter.
4. The “+” ① and “-” ② keys change the parameter.
5. Pressing the Menu key ③again saves the settings.
Backside, bottom connections
①+ Button
②– Button
③Menu button
④USB (type A)
For external devices.
Example: Power for active
loudspeakers. USB keyboard for
host device.
⑤
Audio output
For active
speakers
⑥
USB C (type C)
Power from
external power
adapter; DC 5V
3.0A
⑦
USB C (type C)
Touch screen
control for host
device (MVR
devices) and
USB type C
graphical signal
(video signal) and
USB power from
host device.
⑧
HDMI (type A)
Graphical signal /
video signal from
host device.
HDMI 1.4, supports
HDCP 1.4 for audio,
supports DVI via
adapter.
Back Panel - Connections

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Back Panel - VESA Mount
Troubleshooting
Issue or Problem: Possible reason and solution:
The display of the monitor remains black, or the display
ashes, although it is connected correctly.
The graphical video output of your host device may be
outside the specication for this MTS. (See Appendix A).
Please check resolution settings and framerate of your device.
The power of the USB port of your host device may not be
sufcient to operate the monitor via USB.
1. Please set the brightness of the MTS display in the menu to
50% (value 5 of 10) and turn on the host device again.
2. If this measure is not sufcient, or you cannot see the
settings menu clearly, please connect the external USB
power adapter, included with the MTS156 monitor, to the
second USB (type C) port of the monitor. (Number ⑥in the
connection diagram, Backside, bottom connections section).
An external power supply was connected to the
MTS monitor. The MVR recorder can no longer be
switched off.
The MTS monitor now supplies power to the back of the
MVR recorder via USB. Even if you switch off the recorder,
it remains active.
The recorder turns off when the whole system is without power.
In this case you should turn off your video cart (the complete
system) when not in use.
The monitor back is VESA 75 and VESA 100 compatible and easily attaches to a matching monitor mount. M4 screws are usually
supplied with the monitor mount.
• The thread depth of the monitor is 8mm.
• The open thread length of the fastening screw must not
be less than 7mm.
Note: Please use M4x10mm screws and a VESA plate whose thickness does not exceed 3mm.

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Appendix A: MTS156 Specications
Function Monitor with touchscreen function.
Case Aluminum Alloy
Touch function Capacitive Touch
Screen Size 15.6” diagonal (w x h: 344,2 x 193,6 mm)
Screen Resolution 1920 x 1080
Brightness 320 cd/m2
Contrast Ratio 800 (typ)
Response Time 16 ms (typ)
View Angle 80o/ 80o/ 80o/ 80o
Number Of Touch Points 10
Video Input HDMI 1.4 (type A)
HDMI 1.4, support HDCP 1.4, support of DVI via adapter
Supports HDMI and DVI from host device
Supported resolutions:
3840x2160p30/25,
1920x1080p60/50/30/25/i60/i50,
1280x720p60/50
USB Ports 2x USB type C (USB C3.1)
1x USB type A (USB A2.0)
Audio Output 1x 3.5mm (3pole TRS)
Mechanical Dimensions (w x h x d): 357.1 x 224.9 x 18 mm / 14 x 8.9 x 0,7“
Weight 0,97 kg (2.14 lbs)
Environmental Operating: ambient temperature -10° to +40° C,
air pressure 700 to 1060hPa, humidity 30 to 90% (non-condensing)
Storage and transportation: ambient temperature -20° to +80° C,
air pressure 700 to 1060hPa, humidity 10 to 95% (non-condensing)
Protection against electric shock SELV (Safety Extra Low Voltage)
Ingress protection.
Protection against penetration
of objects and liquids
IP20 (= not protected)
Solid particle protection: 2 = Fingers or similar objects
Protection against harmful ingress of water: 0 = None
Degree of protection in the
presence of ammable mixtures
This device is not protected against explosions.
(Do not operate this device in ignitable atmosphere)
Power DC 5V / 3A
USB-Type C / or external Power supply
Power consumption: 15 Watt max (7W typ)
Box Contents MTS monitor, HDMI cable, 1 x USB A to USB C cable, 2x USB C cable, Power Supply,
Instructions for Use (English)

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Compliance and
Certication
Medical Equipment Safety:
EU: EN 60601-1: 2006+A1:2012+A12:2014+A2:2021
UK: BS EN 60601-1: 2006+A1:2012+A12:2014+A2:2021
US: AAMI ES60601-1:2005+A1:2012+A2:2021
Electromagnetic Compatibility EMC:
EN 60601-1-2:2015+A1:2021
Low Voltage Directive: (2014/35/EU)
Classication Class I Equipment / Mode of operation: continuous
No AP/APG. No Applied Part.
Quality Management
Standard
ISO 13485
Classication of
host device
Class I Equipment (e.g. MediCapture MVR / MVR Lite)
Classication of
mounting device
Class I to comply with 60601-US deviation
Compliance / Certication / Classication
Medical Device Regulation (EU) 2017/745
Conformité Européenne
(European Conformity)
UKCA marking
(UK Conformity Assessed. Product conforms to the requirements of the UK MDR 2002 for
Class 1 devices)
WEEE compliant
RoHS compliant
This device complies with FCC CFR Title 47 - Part15 - Subpart B of the FCC emission Rules.
Note: These specications are subject to change without notice.

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Warranty Conditions
If, during the year that immediately follows the purchase date, a product covered by this warranty is found to have a defect in
material or workmanship, MediCapture (or a service facility authorized by MediCapture) will restore the product to its original
operating condition without charge for parts or labor. Note: MediCapture reserves the right to utilize reconditioned subassemblies as
warranty replacements.
This warranty applies only to those products sold by retailers authorized by MediCapture to sell such products and is enforceable by
the original purchaser only.
THIS WARRANTY IS APPLICABLE IN THE FIFTY (50) STATES OF THE USA AND THE DISTRICT OF COLUMBIA ONLY. IT
IS NOT APPLICABLE IN THE POSSESSIONS OR TERRITORIES OF THE USA OR IN ANY OTHER COUNTRY. THIS IS THE
ONLY EXPRESS WARRANTY WHICH MEDICAPTURE MAKES IN CONNECTION WITH THE ABOVE LISTED PRODUCT(S).
ANY IMPLIED WARRANTIES APPLICABLE TO THESE PRODUCTS ARE LIMITED TO THE DURATION OF THE EXPRESS
WARRANTY. MEDICAPTURE SHALL NOT BE LIABLE FOR LOSS OF REVENUES OR PROFITS, INCONVENIENCE, EXPENSE
FOR SUBSTITUTE EQUIPMENT OR SERVICE, STORAGE CHARGES, LOSS OR CORRUPTION OF DATA, OR ANY OTHER
SPECIAL, INCIDENTAL, OR CONSEQUENTIAL DAMAGES CAUSED BY THE USE OR MISUSE OF, OR INABILITY TO USE,
THE ABOVE LISTED PRODUCT(S), REGARDLESS OF THE LEGAL THEORY ON WHICH THE CLAIM IS BASED, AND EVEN
IF MEDICAPTURE HAS BEEN ADVISED OF THE POSSIBILITY OF SUCH DAMAGES. IN NO EVENT SHALL THE RECOVERY
OF ANY KIND AGAINST MEDICAPTURE BE GREATER IN AMOUNT THAN THE PURCHASE PRICE OF THE PRODUCT(S)
LISTED ABOVE AND CAUSING THE ALLEGED DAMAGE. WITHOUT LIMITING THE FOREGOING, YOU ASSUME ALL RISK
AND LIABILITY FOR LOSS, DAMAGE OR INJURY TO YOU AND YOUR PROPERTY AND TO OTHERS AND THEIR PROPERTY
ARISING OUT OF USE OR MISUSE, OR INABILITY TO USE, THE ABOVE LISTED PRODUCT(S) NOT CAUSED DIRECTLY BY
THE NEGLIGENCE OF MEDICAPTURE (some STATES DO NOT ALLOW LIMITATIONS ON HOW LONG AN IMPLIED WARRANTY
MAY LAST, OR DO NOT ALLOW THE EXCLUSION OR LIMITATION OF INCIDENTAL OR CONSEQUENTIAL DAMAGES, SO THE
ABOVE EXCLUSION OR LIMITATION MAY NOT APPLY TO YOU).
This warranty gives you specic legal rights. You may also have other rights which vary from state to state. In the event any of the
provisions of this warranty are found to be unenforceable, all remaining provisions shall retain full force.
Owner Responsibilities
■Read the Instructions for Use completely.
■Warranty registration is not necessary. However, should warranty service be required, you must be able to provide proof
of the purchase date and the identity of the seller who made the sale (either MediCapture or an authorized reseller).
Please save your sales receipt and invoice.
■Make sure that the proof of purchase that you save contains the serial number and that it matches the number on the
unit that you purchased.
■Depending on where you purchased your unit, promptly notify either MediCapture or the authorized reseller of any
malfunction upon discovery.
■In the event service is required, return the product to an authorized MediCapture service center. All shipments must
be PREPAID. No COLLECT shipments will be accepted. Products repaired under warranty by MediCapture, or an
authorized service center, will be returned to the sender PREPAID.
■Products returned for service (in or out of warranty) MUST have a Return Merchandise Authorization (RMA) number
issued by MediCapture or an authorized service center.
Exclusions
IMPORTANT: The following conditions can cause this warranty to be unenforceable.
■Purchase of the product listed above from resellers NOT authorized by MediCapture to sell the product.
■ Alteration or removal of the trademark, name, or identication number or serial number of the products.
■Use of parts or supplies (other than those sold by MediCapture) that cause damage to the products.
■ Product failures that are the result of: neglect, abuse, misuse, modication, or accidental damage
©2023 MediCapture Inc.
Appendix B: MediCapture Limited Warranty
MediCapture Inc. (“MediCapture”) warranties the product(s) listed below to be free of defects in materials and workmanship for a
period of one (1) year. Should warranty service be required, the warranty period will be extended by the number of days required to
restore normal operation and return the product(s).
MediCapture MTS156 Monitor with Touch Screen