User's Manual

CPR4 – UA10821A

For the same reason, if the CPR4 does not turn on, check at first that the USB cable is properly and completely

inserted into a working USB port of the programmer. Also, try changing ports.

5.3 UPGRADE OF THE PROGRAMMING HEAD’S SOFTWARE

The CPR4 contains a dedicated embedded software. When a new release of this software is available, it will be

included in a comprehensive upgrade of the programmer’s software (SmartView).

In this case, the first time the head is connected to the programmer after the SmartView upgrade, its software is

automatically updated. During this task, the white LEDs on the CPR4 will illuminate in circle, one after the other,

while a message on the screen informs the user about the progression.

6 MAINTENANCE

6.1 Cleaning

The CPR4 should never be immersed in any liquid or cleaned with sterilization products. Avoid spilling liquid

on the equipment.

In order to clean the CPR4:

1. Visually inspect it for contaminants and remove loose material with a dry or water-moistened cloth.

2. Then clean it with a tissue pad or a wipe moistened with one of the following agents:

 Ethyl alcohol

 Isopropyl alcohol

The above-mentioned agents have been tested by the manufacturer, and validated to neither cause physical damage

nor degradation to the CPR4.

6.2 Disinfection and sterilization

The CPR4 is delivered non sterile, and cannot be disinfected or sterilized. It must be covered with a sterile

sleeve when using in sterile environments.

6.3 System end-of-life

At its end of life, the CPR4 shall be sent back to the manufacturer for recycling.

6.4 Regular maintenance

All of the tasks relative to regular (i.e. periodical, preventive) maintenance of CPR4 consist of cleaning the outer

surfaces.

Please note that, in some jurisdictions, local regulation may require the execution of some specific safety inspections.

It is recommended to visually inspect the CPR4 before use.

In case of any visible damage, please contact your MicroPort representative.

7 GUIDANCE AND MANUFACTURER'S DECLARATION

All information below is based on the normative requirements to which the manufacturers of electro-medical devices

are subject, in the sense of IEC60601-1-2.