Mindray Animal Medical Technology AP-6 Wireless Access Point User Manual

Mindray Animal Medical Technology AP-6 Wireless Access Point

Product Information

The AP-6 is a wireless access point designed for veterinary use. It is manufactured by SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. The product is intended to be used in animal medical institutions such as wards, postoperative observation rooms, and ICU/CCU. It is important to note that the product is for veterinary use only.

Intellectual Property Statement
The AP-6 is a trademark of SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. in China and other countries. All other trademarks mentioned in the manual are used for informational or editorial purposes and belong to their respective owners.

Responsibility on the Manufacturer Party
Mindray Animal Medical, the manufacturer of the AP-6, is responsible for conducting authorized personnel for the product, ensuring electrical installation compliance with national and local requirements, and ensuring the product is used according to the instructions for use.

Warranty
The warranty provided for the AP-6 is exclusive and replaces all other warranties, expressed or implied, including warranties of merchantability or fitness for any particular purpose.

Exemptions
The warranty does not cover unauthorized service by non-authorized personnel, malfunction of instruments or parts with illegible serial numbers or issues not caused by the instrument or part itself.

Company Contact
Manufacturer: Shenzhen Mindray Animal Medical Technology Co., Ltd.
Address: Room 702, Tower 4, YESUN Intelligent Community III, No.130188 Guanguang Road, Xinlan Community, Guanlan Street, Longhua District, Shenzhen 518110, P. R. China
Website: www.mindrayanimal.com
Email Address: service@mindrayanimal.com
Tel: +86 755-33997000

Preface

• Manual Purpose: The purpose of this manual is to provide instructions for clinical professionals with a working knowledge of medical procedures, practices, and terminology required for monitoring critically ill patients.
• Intended Audience: This manual is intended for clinical professionals who will be using the AP-6 in their medical practice.

Illustrations
All illustrations in the manual are provided as examples only and may not reflect the setup or data displayed on the actual equipment.

Conventions
Italic text is used to quote referenced chapters or sections in the manual. Bold text is used to indicate screen texts. <code> is used to indicate operational procedures.

Product Usage Instructions

Product Overview
Intended Use
The AP-6 wireless access point is designed for use in veterinary medical institutions, such as wards, postoperative observation rooms, and ICU/CCU. It is used to connect the telemetry monitoring device to the central monitoring system.

Appearance
The AP-6 has a specific appearance that is not described in detail in the user manual. Please refer to the product itself for its physical appearance.

Indicator Status
The user manual does not provide specific information about the indicator status of the AP-6. Please refer to the product or contact the manufacturer for more information.

Equipment Preparation
The user manual does not provide information on equipment preparation. Please refer to the manufacturer’s instructions or contact their support for guidance on equipment preparation.

Interconnected Monitoring
The user manual does not provide information on interconnected monitoring. Please refer to the manufacturer’s instructions or contact their support for guidance on interconnected monitoring.

Fault Rule Out
The user manual does not provide information on fault rules. Please refer to the manufacturer’s instructions or contact their support for guidance on fault rule-out.

Product Specifications
The user manual does not provide specific product specifications. Please refer to the manufacturer’s instructions or contact their support for detailed product specifications.

EMC and Radio Management Compliance
The user manual does not provide information on EMC and Radio Management Compliance. Please refer to the manufacturer’s instructions or contact their support for guidance on EMC and Radio Management Compliance.

IMPORTANT!
The product is for veterinary use only.

Intellectual Property Statement
Shenzhen Mindray Animal Medical Technology Co., Ltd. (hereinafter called Mindray Animal Medical) owns the intellectual property rights to this product and this manual. This manual may refer to information protected by copyright or patents and does not convey any license under the patent rights or copyright of Mindray Animal Medical, or of others. Mindray Animal Medical intends to maintain the contents of this manual as confidential information. Disclosure of the information in this manual in any manner whatsoever without the written permission of Mindray Animal Medical is strictly forbidden. Release, amendment, reproduction, distribution, rental, adaptation, translation or any other derivative work of this manual in any manner whatsoever without the written permission of Mindray Animal Medical is strictly forbidden. is the trademark of SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. in China and other countries. All other trademarks that appear in this manual are used only for informational or editorial purposes. They are the property of their respective owners.

Responsibility on the Manufacturer Party
Contents of this manual are subject to changes without prior notice. All information contained in this manual is believed to be correct. Mindray Animal Medical shall not be liable for errors contained herein nor for incidental or consequential damages in connection with the furnishing, performance, or use of this manual.

Mindray Animal Medical is responsible for the effects on safety, reliability and performance of this product, only if:

• All installation operations, expansions, changes, modifications and repairs of this product are conducted by Mindray Animal Medical authorized personnel;
• The electrical installation of the relevant room complies with the applicable national and local requirements;
• The product is used in accordance with the instructions for use.

Warranty

THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR PURPOSE.

Exemptions
Mindray Animal Medical’s obligation or liability under this warranty does not include any transportation or other charges or liability for direct, indirect or consequential damages or delay resulting from the improper use or application of the product or the use of parts or accessories not approved by Mindray Animal Medical or repairs by people other than Mindray Animal Medical authorized personnel.
This warranty shall not extend to

• Malfunction or damage caused by improper use or man-made failure.
• Malfunction or damage caused by unstable or out-of-range power input.
• Malfunction or damage caused by force majeure such as fire and earthquake.
• Malfunction or damage caused by improper operation or repair by unqualified or unauthorized service people.
• Malfunction of the instrument or part whose serial number is not legible enough.
• Others not caused by the instrument or the part itself.

Company Contact

Manufacturer : Shenzhen Mindray Animal Medical Technology Co., Ltd.
Address : Room 702, Tower 4, YESUN Intelligent Community III, No.1301- 88 Guanguang Road, Xinlan Community, Guanlan Street, Longhua District, Shenzhen 518110, P. R. China
Website : www.mindrayanimal.com
E-mail Address service@mindrayanimal.com
Tel : +86 755-33997000

Preface

Manual Purpose
This manual contains the instructions necessary to operate the product safely and in accordance with its function and intended use. Observance of this manual is a prerequisite for proper product performance and correct operation and ensures patient and operator safety. This manual is based on the maximum configuration and therefore some contents may not apply to your product. If you have any question, please contact us. This manual is an integral part of the product. It should always be kept close to the equipment so that it can be obtained conveniently when needed.

Intended Audience
This manual is geared for clinical professionals who are expected to have a working knowledge of medical procedures, practices and terminology as required for monitoring of critically ill patients.

Illustrations
All illustrations in this manual serve as examples only. They may not necessarily reflect the setup or data displayed on your equipment.

Conventions

• Italic text is used in this manual to quote the referenced chapters or sections.
• Bold text is used to indicate the screen texts.
•  → is used to indicate operational procedures.

Product Overview

Intended Use
This product is applicable to the wireless access point where the telemetry monitoring device connects to the central monitoring system.
The product is intended to be used in animal medical institutions, such as wards, postoperative observation rooms, and ICU/CCU.

Appearance Figure 2 Back View

Status
4.| LAN port| For POE input power supply and Ethernet communication
5.| Key| In the connected switch state, press and hold the key to restore the AP to the default network configuration.
6.| Antenna| Used for communication with the telemetry transmitter, sending and receiving data.

Indicator Status
The indicator status is stable after AP power-on. The color change is as follows:

n  On: Steady green

n  Off: Off

n    On: Off

n    Off: Off

RF indicator (Load indicator)| To connect the telemetry transmitter:

n  On: Steady blue

n  Off: Off

Not connecting the telemetry transmitter:

n  On: Steady green

n  Off: Off

Run indi:ator (Status indicator)| DHCP failure:

n  On: Steady red

n  Off: Steady red

Connection with ACconnected

n  On: Steady red

n  Off: Steady red

AC Connected Successfullswitch

n  On: Steady green

n  Off: Off

Power-on self-test failed

n  On: Steady red

n  Off: Steady red

Getting Started

Environmental Requirements
The operating environment of the equipment must comply with the environmental specifications of the telemetry monitoring system for livestock use. Avoid noise, vibration, dust, corrosive, flammable and explosive substances.
After the installation of this device is completed, it is forbidden to transfer the device to another environment to avoid that the device cannot work normally due to environmental reasons. To transfer the device, please contact the service engineer or your agent.

Power Supply Mode

The device is powered by POE through a switch and is connected to the switch using a network cable.

• Input voltage: 36-57 V DC
• Input current: 0.35-0.1 A

Connection
See the AC Configuration Tool Installation and Use Guide and Wireless Survey Tool Installation and Use Guide.

Startup
After connecting to a switch that supports POE power supply, the device automatically starts up. After startup, the LED on the front of the device flashes and the status of the LED is red in the middle and green on both sides.

Work Mode
The device can operate in two modes:

• Normal work mode: Run indicator: Green. In this mode, the AP provides hotspots for connection. The user uses the TMS30 Vet and TMS30A Vet to connect the AP, and the AP transmits the wireless received data to the central monitoring system through a network cable.
• Abnormal mode: The RUN indicator is red. In this mode, the AP cannot connect to the telemetry monitoring device. The user needs to configure the channel and SSID in the AC configuration tool and turn on the RF switch.

Networked Monitoring

This device is connected to the CMS through a switch and AC. After the CMS is connected, the real-time data detected on the telemetry box will be uploaded to the CMS through this device and displayed on relevant screens of the CMS.

Troubleshooting

The following table lists some of the most common failures that may occur with this device. If the problem persists, contact our customer service engineer or your local distributor.

verification

n   Network cable failure

| 1.          Replace thSSIDsettingidoesnotmatchtha tthetelemetrybox

2.          Replace the network cable.

The telemetry box cannot be connected in Work Mode mode.| n   There is interference from other devices of the same frequency band in the operating environment.

n   Thdistancebetween of AP does not match that of the telemetry

boxAPtoolong,resultingt oolowoftelemetrybox.

| 1.          Turn off other devices in the current environment.

2.          Restart the telemetry box.

The CMS data is disconnected continuously.| n   There is interference from other devices of the same frequency band in the operating environment.

n   The distance between the telemetry box and the AP is too long, resulting in too low

Signal Level of the telemetry bonormal

| 1.          Turn off other devices in the current environment.

2.          Pport the telemetry box close to the AP to check whether it is normal.

Product Specifications

Product Classification

Degree of protection against electrical shock| Information technology equipment, class III
---|---
Degree of protection against harmful ingress of water| IPX1

Environmental Specifications

Power Specifications

Physical Specifications

Hardware Specifications

Key

Reset key| 1
External interfaces
LAN port| 1
---|---
Micro USB Interface| 1
Antenna| 2

WMTS Specifications

central

monitoring system: ≤ 3 s

System capacity| Maximum capacity in single AP:: 3 leads, 1 sets
Wireless coexistence| The TMS30 Vet and its co-channel interference power works properly when the value is -8 dBm.

The TMS30 Vet and its adjacent channel interference power works properly at – 0 dBm.

Network interruption alarm| When the network is interrupted, the CMS triggers a related alarm no more than 8s. After the network recovers, the

wireless connection can be restored automatically.

EMC and Radio Management Compliance

See Veterinary Telemetry System Operator’s Manual.
Caution :
This device complies with  Part  15  and  Part  95  of the  FCC  rules and Industry  Canada license‐exempt RSS standard(s). 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. Any changes or modifications to this equipment not expressly approved by  Shenzhen  Mindray  Animal Medical  Technology Co., Ltd. may cause harmful radio frequency interference and void your authority to operate this equipment.
Installation of this telemetry device is permitted in hospitals and healthcare facilities only. This device shall not be operated in mobile vehicles (including ambulances and other vehicles associated with healthcare facilities). The installer/user of this device shall ensure that it is at least 80 km from the radio astronomy observatories listed below.

• (i) National  Astronomy  and  Ionosphere  Center,  Arecibo,  Puerto  Rico:  18°–20′–38.28′North Latitude, 66°–45′–09.42′ West Longitude;
• (ii) National  Radio  Astronomy  Observatory,  Socorro,  New  Mexico:  34°–04′–43′  North Latitude, 107°–37′–04′ West Longitude; or
• (iii) National  Radio  Astronomy  Observatory,  Green  Bank,  West  Virginia:  38°–26′–08′North Latitude, 79°–49′–42′ West Longitude.

For medical telemetry systems not meeting this  80  km separation  (e.g. the Okanagan  Valley, British Columbia) the installer/ user must coordinate with, and obtain the written concurrence of, the National Science Foundation (NSF) before the equipment can be installed or operated. The National Science Foundation (NSF) point of contact for coordination is: Division of Astronomical Sciences, Electromagnetic Spectrum Management Unit, 2415 Eisenhower Avenue, Alexandria, VA 22314; Email: esm@nsf.gov.

The manufacturer is not responsible for any radio or  TV  interference caused by unauthorized modifications or changes to this equipment. Such modifications or change could void the user’s authority to operate the equipment.
This radio transmitter (identify the device by certification number or model number if Category II) has been approved by Industry Canada to operate with the antenna types listed below with the maximum permissible gain indicated. Antenna types not included in this list, having a gain greater than the maximum gain indicated for that type, are strictly prohibited for use with this device.

This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 and Part 95 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a  residential installation.  This equipment generates,  uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions,  may cause harmful interference to  radio communications.  However,  there is  no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the  equipment  off  and  on,  the  user  is  encouraged  to  try  to correct the  interference  by  one  or  more of the following measures:

• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment and the receiver.
• Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
• Consult the dealer or an experienced radio/TV technician for help.

The device has been evaluated to meet general RF exposure requirements.
To  maintain compliance with  FCC’s  RF  exposure guidelines,  this equipment should be installed and operated with a minimum distance of 20cm between the radiator and your body.

References

• Mindray Animal Medical
• Mindray Animal Medical

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