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Table Of Contents
- POC-621 Series (DC-/ AC-in model)
- Contents
- 1 General Information
- 1.1 Introduction
- 1.2 Specifications
- 1.3 Dimensions
- Figure 1.1 Dimensions of the POC-621
- Figure 1.2 POC-621 Hot Swappable Battery Pack Dimensions
- Figure 1.3 POC-621 with Smart Card Reader Dimensions
- Figure 1.4 POC-621 with RFID & Camera Accessory Dimensions
- Figure 1.5 POC-621 VESA Mounting
- Figure 1.6 POC-621 Series Front Panel
- 1.3.1 Optional Modules
- 1.3.2 Cleaning and Disinfecting the Solution
- 1.4 Operating Principle
- 1.5 Intended User Profile
- 1.6 Front Bezel Button
- 2 System Setup
- 3 Hot Swapping Battery Pack Operation
- 4 Operation and Safety
- A POC-621 Series VESA Mounting
- B Driver Installation
- C PCM-8722 Connector Map
- D PCM-8722 Jumper Settings
- D.1 PCM-8722 Jumper setting
- Table D.1: CN3 ME Manufacturing Mode
- Table D.2: CN5 Clear CMOS
- Table D.3: CN6 (Not Install) Clear ME
- Table D.4: CN8 (Not Install) System Reset
- Table D.5: CN13 LVDS Voltage Setup
- Table D.6: CN40 Power Button (Internal Test Only)
- Table D.7: PCN4 Power Debug (Reserved)
- Table D.8: SW1 Board Setup
- Table D.9: SW1 Pin 4 Speaker Function
- Table D.10: SW2 Panel Resolution/Type Setup
- D.1 PCM-8722 Jumper setting
- E Advanced BIOS Functions
v POC-621 Series User Manual
15. Accessory equipment connected to the analog and digital interfaces must be in
compliance with the respective nationally harmonized IEC standards (i.e. IEC
60950 for data processing equipment, IEC 60065 for video equipment, IEC
61010-1 for laboratory equipment, and IEC 60601-1 for medical equipment.)
Furthermore all configurations shall comply with the system standard IEC
60601-1-1. Everybody who connects additional equipment to the signal input
part or signal output part configures a medical system, and is therefore, respon-
sible that the system complies with the requirements of the system standard IEC
60601-1-1. The unit is for exclusive interconnection with IEC 60601-1 certified
equipment in the patient environment and IEC 60XXX certified equipment out-
side of the patient environment. If in doubt, consult the technical services
department or your local representative.
16. Grounding reliability can only be achieved when the equipment is connected to
an equivalent receptacle marked "Hospital Only" or "Hospital Grade".
17. Use a power cord that matches the voltage of the power outlet, which has been
approved and complies with the safety standard of your particular country.
18. WARNING - Do not modify this equipment without authorization of the manufac-
turer.
19. WARNING - To avoid risk of electric shock, this equipment must only be con-
nected to a supply mains with protective earth.
20. CAUTION: This adapter Sinpro HPU101-107 is a forming part of the medical
device.
21. Remove the power cord to fully turn off the device.
Instructions pour l'utilisateur
Le document combine du texte et des illustrations, offrant un aperçu complet du sys-
tème. Les informations sont présentées sous forme d'actions séquentielles, permet-
tant à l'utilisateur d'apprendre directement à utiliser le périphérique.
Le texte fournit des explications et informe l'utilisateur, étape par étape, de l'utilisation
pratique du produit, avec des instructions courtes et claires, dans une séquence fac-
ile à suivre.
Caution! Use a suitable mounting apparatus to avoid risk of injury.
Note! Environmental protection
Follow national requirements when disposing of this unit.