DentalEZ Core Manuel utilisateur

CORETM Delivery Unit

Console Mount

User Manual

www.DentalEZ.com 866-DTE-INFO

DentalEZ®Equipment

PN: 2717-269C

Table of Contents

Section I Introduction

Product Overview ............................................... 1

Console Mounted Unit Features........................2

Dimensions ........................................................ 3

Specications .................................................... 4

Classications ................................................... 5

Explanation of Symbols & Signs ...................... 5

Safety Precautions............................................ 6

Section II Preinstallation

Packaging .......................................................... 9

Unit Placement ................................................. 10

Utility Service Center (USC).............................10

Section III Installation

Console Adaptor Mount................................... 13

Console ............................................................. 15

Assistant’s Arm (Optional)............................... 16

Assistant’s Instrumentation............................ 17

Cuspidor (Optional) ..........................................18

Delivery Head Arm Assembly.......................... 19

Light Post (Optional) ........................................ 19

Fiber Optic Electrical (Optional) ..................... 20

Handpiece Tubing ........................................... 20

Finalizing USC Installation ............................... 21

Power Module (Optional)................................. 23

Section IV Testing

Delivery System............................................... 25

Syringe ............................................................. 26

Foot Control and Handpieces......................... 26

Cuspidor........................................................... 28

Other Optional Features.................................. 30

Section V Operation

Delivery Head.................................................... 31

Syringe ............................................................. 32

Foot Control ..................................................... 32

Assistant’s Vacuum Accessories................... 33

Clean Water System........................................ 33

Cuspidor........................................................... 34

Section VI Care

Cleaning ........................................................... 35

Disinfecting...................................................... 36

Section VII User Service Information

Troubleshooting .............................................. 37

Service Instruction .......................................... 40

Disposal of Equipment.................................... 40

Section VIII Parts Lists/Diagrams

Utility Service Center ....................................... 41

Assistant’s Arm (Optional)............................... 41

CORE Delivery Head ........................................ 42

Touch Pads....................................................... 43

Console ............................................................ 44

Simplicity Cuspidor (Optional)........................ 45

Galaxy Cuspidor (Optional) ............................. 46

Foot Control ..................................................... 47

Air/Water Syringe ............................................ 47

HVE Nozzle....................................................... 48

Saliva Ejector Nozzle....................................... 48

EMC Information.............................................. 49

Limited Warranty.............................................. 51

www.DentalEZ.com 866-DTE-INFO

CORETM Console Mounted Unit

PN: 2717-269C

www.DentalEZ.com 866-DTE-INFO

DentalEZ®Equipment

PN: 2717-269C

This manual contains installation, operation and

care instructions, and user service information

for the DentalEZ® CORE™ Console Mounted Unit

(CMU).

The CORE CMU is intended to be used by trained

professional dental care personnel only, as an

interface device to connect the dental operatory

hand instruments to the appropriate supply utility

such as air, water, vacuum, drain and electrical.

It functions as a system management device

that provides a method of operating the hand

instruments from a single control input device.

The CORE CMU is manufactured to be used

with a dental chair that supports a patient in

a reclined seated position. Operators will be

positioned around the patient’s head as required

for optimum access for the specic procedure

being performed. The delivery unit positions the

handpieces for the optimum presentation to the

operator.

The CORE CMU is designed to provide trouble-

free service when installed, operated and cared

for according to the procedures set forth in this

manual.

To ensure proper installation, carefully

read all of the instructions contained in

this manual, paying close attention to all

warnings, cautions and notes.

Before starting installation procedures, review

the illustration to become familiar with the

components of the CORE CMU (Figure 1).

After the CORE CMU is installed, review the

features, operation procedures, and care

guidelines with the doctor’s sta.

Leave this manual in the doctor’s oice.

Section I Introduction

Product Overview

• Installation by an authorized

DentalEZ dealer service technician is

recommended.

• For any questions about an order, please

contact a DentalEZ Equipment customer

service representative at 866-DTE-INFO.

NOTICE

Figure 1. Main components of the CORE CMU

Adjustable

Arm

Light Post

(Optional)

Delivery

Head

Clean

Water

System

www.DentalEZ.com 866-DTE-INFO

CORETM Console Mounted Unit

PN: 2717-269C

Console Mounted Unit Features

Designed with simplicity in mind, the CORE product line provides a straightforward, easy-to-use delivery

unit with common components, simple integrated holders and an easy-to-read pressure gauge. The

console mounted unit positions StarDental® handpieces and ancillaries within easy, comfortable reach.

Standard Features

• Secure tray placement.

• Air gauge for easy pressure monitoring.

• Break release handle.

• Easy access control block and internals

for easy maintenance.

• Aluminum ex arm for stability and ease

of positioning.

• Built standard with BioFreeTM tubing.

Optional Features

• Optional integrated dual access touchpad

controls.

• Rear assistant’s arm/instrumentation

with centrally located solids collector and

tubing.

NOTE: Image shown contains optional

handpieces and upgraded features: Galaxy

Cuspidor, Simplicity Telescoping Assistant

Instrumentation, Unit Touchpad and Wired Foot Control.

Section I Introduction

www.DentalEZ.com 866-DTE-INFO

DentalEZ®Equipment

PN: 2717-269C

Section I Introduction

Dimensions

Figure 2. Top and side view dimensions for the CORE console mounted delivery unit

23½"

7¾"

27½"

19"

15¾" 16¼"

10½" to 23⅞"

6¼"

17½"

21¾"

57"

20¾"

15¼"

16"

18"

22"

www.DentalEZ.com 866-DTE-INFO

CORETM Console Mounted Unit

PN: 2717-269C

Power Supply

• 115V AC, 50/60 Hz, as applicable

Air Pressure

• 551.6 kPa (80 PSI) (at regulator in USC)

Water Pressure

• 275.8 kPa (40 PSI) (at regulator in USC or clean

water manifold)

Clean Water System

• Reservoir capacity: 1.0 L

Shipping (Package) Weight

• CORE Traditional Delivery Head and Arms:

24.5 lb. (11.1 kg)

• Magellan Delivery Unit Post: 13 lb. (5.8 kg)

• Magellan Delivery Unit Support: 20 lb. (9 kg)

• Utility Service Center (USC): 15 lb. (6.8 kg)

• Assistant’s Arm: 16 lb. (7.2 kg)

• Light Post (Optional): 15 lb. (6.8 kg)

Specications

Recommended Environmental Conditions

Transportation and Storage

• Temperature range: -20°F to 165°F

(-29°C to 74°C)

• Relative humidity range: 0% to 95%

Operation

• Conditioned air

• Temperature range: 59°F to 80°F (15°C to 27°C)

• Atmospheric pressure range: 50 to 105 kPa

Section I Introduction

www.DentalEZ.com 866-DTE-INFO

DentalEZ®Equipment

PN: 2717-269C

Section I Introduction

Explanation of Symbols & Signs

Classications

For the purposes of this user manual, the UL

approval is for the unit (head/arm assembly) and

power supply. All other regulatory markings are

provided in their respective manuals.

• Type of Protection Against Electric Shock:

Class 1 Equipment.

• Degree of Protection Against Electric Shock:

Type B Applied Parts. The handpiece is

considered an applied part.

• Degree of Protection Against Ingress of Water:

Ordinary

• Flammable Gases: Equipment not suitable for

use in the presence of a ammable anesthetic

mixture with air, oxygen or nitrous oxide.

• Not intended for use in an oxygen rich

environment.

• Mode of Operation: Continuous

Medical-General Medical Equipment

Certied as to electrical shock, re

and mechanical hazards only in

accordance with:

ANSI/AAMI ES60601-1:2005

CAN/CSA C22.2 NO. 60601-1-08

IEC 80601-2-60:2012

53HN

E355890

The authorized European representative is:

Dental Hygienics & Decontamination (DHD)

41 Blackwell Drive, Braintree Business Park

Braintree Essex, CM7 2PU, UK

Phone: +44 01787 877877 (ext. 200)

= Caution

= Warning

= Biohazard

= Warning - Dangerous Voltage

= General Mandatory Action

= Refer to Manual (Follow Instructions)

= Alternating Current

= Direct Current

= Protective Earth (Ground)

= Type B Applied Part

= European Certication

= Serial Number

= Manufacture Date

= Manufacturer

= Electromagnetic Radiation

= Do Not Trash

= Box Must Remain Upright

= Do Not Place Box on Unlevel Surface

= Do Not Stack Box

= Box Contents Safe Temperature Range

= Box Contents Safe Humidity Range

www.DentalEZ.com 866-DTE-INFO

CORETM Console Mounted Unit

PN: 2717-269C

Section I Introduction

Safety Precautions

To satisfy FCC RF exposure requirements

for mobile and base station transmission

devices, a separation distance of 20 cm or

more should be maintained between the

antenna of this device and persons during the

operation. To ensure compliance, operation at

closer that this distance is not recommended.

The antenna(s) used for this transmitter must

not be co-located or operating in conjunction

with any other antenna or transmitter.

CAUTION

• Some illustrations and instructions in

this user manual include installation of

optional city water. If optional city water

is wanted, purchase kit PN 3658-455 for

units with a cuspidor or PN 3658-456 for

units without a cuspidor.

• Isolating the unit from the supply mains is

accomplished by unplugging the unit from

the power receptacle.

NOTICE

Before proceeding with electrical

installation, all wiring must be in

accordance with NEC and local electrical

codes.

To avoid the risk of electrical shock, this

equipment must only be connected to a

supply mains with protective earth.

• Do not modify this equipment without

permission from DentalEZ. Unauthorized

modication will void the warranty and

could result in serious injury. If this

equipment is modied, appropriate

inspection and testing must be conducted

to ensure continued safe use of

equipment.

• Property damage and/or personal injury

may result if directions are not followed or

OEM parts are not used.

• The use of ACCESSORY equipment not

complying with the equivalent safety

requirements of this equipment may lead

to a reduced level of safety of the resulting

system. Consideration relating to the

choice shall include:

• Use of the accessory in the PATIENT

VICINITY

• Evidence that the safety certication

of the ACCESSORY has been

performed in accordance to the

appropriate IEC 60601-1 harmonized

standard.

• Always turn ounit and remove power

from unit when servicing. (Turn opower

at disconnect or service breaker.

• Never leave children unattended when

unit is in use.

WARNING

www.DentalEZ.com 866-DTE-INFO

DentalEZ®Equipment

PN: 2717-269C

Section I Introduction

Safety Precautions (Continued)

• Medical electrical equipment needs

special precautions regarding

electromagnetic (EMC) compatibility

and needs to be installed according to

EMC information. (See EMC Information

provided in this manual.)

• In accordance with Part 15 of FCC rules,

this equipment was tested and complies

with Class A digital device limits. These

limits are designed to give equipment

reasonable protection against

detrimental interference when operated

in a commercial environment.

• Mobile radio frequency (RF)

communications equipment can aect

medical electrical equipment.

• Accessory equipment not complying with

the Medical Device Safety standard IEC

60601-1 may contribute to a reduced level

of safety of the CORE Delivery Unit. It is

necessary for all accessory equipment

and attachments to comply with IEC

80601-2-60 Medical Electrical Equipment.

NOTICE

This equipment has been tested and found

to comply with the limits for a Class B

digital device, pursuant to Part 15 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 o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 receiver.

• Connect the equipment to an outlet on

a circuit dierent from that to which the

receiver is connected.

• Consult the dealer or an experienced

radio/TV technician for help.

NOTICE

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