Ivoclar digital PrograPrint PR5 Manual

ivoclardigital.com
PrograPrint PR5
Short Instructions | Instruções de Uso Resumidas |
Guia breve


Table of Contents | Lista de Conteúdo | Índice
4

English
5
English
1 About this document
These Short Instructions are part of the overall documentation for the device. They are only
valid in combination with the Operating Instructions of the device (“Document of equal
applicability and required files”, page 7).
WARNING! Improper use of the device.
Risk to the patient and the user.
The Short Instructions contain important information on the safe handling of the device:
Operating Instructions and Short Instructions must be read thoroughly prior to
installation and operation.
These Short Instructions will help you to quickly familiarize yourself with the use of
PrograPrint PR5.
Should you lose these Short Instructions, you can download them from
www.ivoclarvivadent.com.
1.1 Signs and symbols
1.1.1 Warnings and additional information
Warnings
Warnings are used in these Operating Instructions to warn you of a risk of injury to persons
and/or damage to property.
1. Please always read and observe these warnings.
2. Follow all measures marked with the warning symbol and warning word.
Depending on the severity and probability of the danger, the following warning levels are
distinguished:
Warning
symbol Warning word Danger level
Consequences resulting
from non-observance
DANGER Immediate imminent
danger
Death, severe personal
injury
WARNING Potential danger Death, severe personal
injury
CAUTION Potential danger Slight personal injury
- NOTICE Potential danger Damage to property

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Explanation of the structure of a warning:
WARNING WORD! Name of source of danger, cause of hazard or type of risk.
Consequences of non-compliance with instructions.
Action in order to avoid danger.
Example of a warning:
WARNING! Risk of injury due to heavy lifting.
Injuries to the back due to overloading.
Only lift the device with the aid of the pallet truck.
Unpack the device only after transportation.
Additional information
Symbol Meaning
Additional information, e. g. for better understanding, for simplifying work
flows or for further information.

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7
1.2 Document of equal applicability and required files
For details on the documents of equal applicability, please contact your local trade partner or
go to the download section of Ivoclar Vivadent at http://www.ivoclarvivadent.com.
In the download area, you can find additional files, such as :
•Installation file for the software “PrograPrint Manager”
•Build styles for the software “CAMbridge”
•DME file for the software “Dental System”
Document Explanation
Operating Instructions
PrograPrint PR5
Comprehensive information on the use of
PrograPrint PR5
Instructions for Use for the
different materials
Information about the use of the materials to be
processed
Operating Instructions for the
cleaning unit PrograPrint Clean
Information about requirements that must be
observed for the transport, set-up and use of
PrograPrint Clean
Operating Instructions for the
post-curing unit PrograPrint Cure
Information about requirements that must be
observed for the transport, set-up and use of
PrograPrint Cure
CAMbridge flow chart Short Instructions for the CAM software
"CAMbridge"
Instructions for Use for
CAMbridge
Manual for the CAM software "CAMbridge"
Short Instructions for:
•PrograPrint PR5
•PrograPrint Clean
•PrograPrint Cure
Excerpt of operation-relevant topics from the
respective Operating Instructions

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2Safety
WARNING! Improper use of the device.
Hazard to the user.
The safety chapter contains important information on the safety of the device: Please read
it thoroughly prior to installation and operation.
The device is built according to state-of-the-art technology and recognized safety regulations.
Nevertheless, operation bears the risk of injury for the user or third parties. Moreover,
impairments to the device and other property are possible.
2.1 Intended use
PrograPrint PR5 has been designed for 3D printing in dental technology using the following
materials:
•ProArt Print Wax (burn-out material for the press and casting technique)
•ProArt Print Model (material for the fabrication of the dental working models)
•ProArt Print Splint (material for the fabrication of dental drilling templates and splints)
Use PrograPrint PR5 exclusively for this purpose.
In the case of damage caused by improper use or failure to observe the Operating Instructions,
all liability and guarantee claims are void.
Please note that only the materials and cleaning agents approved by the manufacturer ensure
processing without damage to the machine.
Only approved materials can be identified by the PrograPrint PR5 by means of the
corresponding RFID code on the material bottle and on the cartridge and used accordingly so
that misapplication is virtually impossible.
All information regarding material and indication extensions corresponds to the state of
knowledge at the time of going to print. For additional details, go to http://
www.ivoclarvivadent.com.
The use of materials from other manufacturers is not recommended due to the lack of
coordination with the printing/fabrication process.

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2.1.1 Potential improper use
The device is not suitable for 3D printing procedures outside of the dental field.
The following is considered as misuse of the system:
•Non-compliance with the specified intended use, intended operator specifications or
intended environment
•Modifications, maintenance and repairs without prior authorization by Ivoclar Vivadent
•Operation with inappropriate parameters
Improper use of the devices can lead to the following:
•Danger for patients and operating personnel
•Impairment of the operability of the devices
Ivoclar Vivadent assumes no liability for damage resulting from improper use.
Typical misapplications of the device to be avoided:
2.1.2 Intended user
The device may only be operated by dental technicians and qualified dental staff for the
fabrication of dental objects for dental applications.
The user is responsible for selecting the correct device settings.
Improper use Consequences
Use of non-approved materials The device cannot execute any printing
orders
Incorrect cleaning and disposal (build
platform, build chamber, hood etc.)
•Skin irritations
•Environmental damage
•Damage to the device
Operation without cartridge or build
platform
Damage to the device
Operation with incorrectly inserted
cartridge or build platform
•Damage to the device
•Deficient printed object
Shut-down of the device by the user during
printing
Deficient printed object
Mixing of different materials •Damage to the patient's health
•Cross-contamination of materials
•Deficient printed object
•Damage to the material, cartridge and
material bottle

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2.1.3 Intended environment
The device is only permitted for use in closed rooms within the specified ambient conditions
(see technical data in the Operating Instructions, “Document of equal applicability and
required files”, page 7) and in compliance with the requirements for safe installation (see
requirements regarding the location site, “Document of equal applicability and required
files”, page 7).
2.2 Operator's obligations
The operator is responsible for the safe operation of the device.
Ensure compliance and control:
a. Intended use
b. Statutory or other safety and accident prevention regulations
Only operate the device in a technically perfect condition, in a proper, safety-conscious
and risk-conscious manner and while observing the Operating Instructions (“Document of
equal applicability and required files”, page 7).
Keep these instructions and all documents of equal applicability complete, legible and
accessible to the personnel at all times.
2.3 Personnel qualifications
Ensure that the personnel assigned to work with the device have read and understood
these instructions and all documents of equal applicability, in particular safety,
maintenance and repair information, before starting to work.
Ensure that personnel is aware of hazards and safety equipment (“Working areas,
potential hazards and safety measures on the device”, page 12).
Manage the responsibilities, competence and monitoring of staff.
All work must only be carried out by qualified technical staff.
Personnel to be trained should only be working with the device under the supervision of
qualified technical staff.
2.4 Staff obligations
Only operate the device in a technically perfect condition, in a proper, safety-conscious
and risk-conscious manner and while observing the Operating Instructions (“Document of
equal applicability and required files”, page 7).
Refrain from any process that could endanger staff or third parties.
In the case of safety-related malfunctions, switch off the device immediately and allow the
fault to be rectified by the person responsible.
In all cases of doubt regarding the safety of the appliance, switch off the appliance and
prevent further use.
In addition to the overall documentation, legal or other safety and accident prevention
regulations including applicable standards and guidelines of the country in which the
device is operated must be complied with.
Do not wear jewellery such as rings, bracelets or watches when working on the appliance,
especially when cleaning the build chamber, to prevent cutting injuries or bruising.

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2.5 Personal protective equipment
If loud operating noises cannot be prevented, use hearing protectors during printing.
For the protection against material and cleaning agent vapours or other dental material
particles while working with cartridges or material bottles or during cleaning, wear
protective masks (half mask with protection class FFP3), gloves and protective gear
suitable for the respective material (see also Instructions for Use or the materials,
“Document of equal applicability and required files”, page 7).

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2.6 Working areas, potential hazards and safety measures on the device
As an operator, you are working at the areas described below.
The device is built according to state-of-the-art technology and recognized technical safety
regulations. Hazardous areas, which cannot be avoided by design, are equipped with
appropriate protective devices. Nevertheless, if the machine is used improperly, there is a
danger to life or risk of injury to the user or third parties. In addition, the devices or dental
applications may become damaged.
The working areas, their potential hazards and applicable safety measures are shown below:
The hood (1) of the printer can only be opened once the build platform (2) is in the home
position (highest position) after a print job as depicted. As soon as the movement of the build
platform is complete, the hood is automatically unlocked.
1
2
3
4

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No.
Working
area Tasks / Work Type of hazard
Safety
equipment
Protective
effect
1 Hood •Access to
the build
chamber
•Mounting
the build
platform
and
cartridge
•Cleaning of
the build
chamber
with the
printer
switched off
Mechanical
hazards
•Safety lock of
the hood.
Access to the
build
chamber is
not possible
while the
build
platform is
moving.
•The printer
does not
start with the
hood open.
Protection
against
crushing
Cushioning of
the hood
against
slamming shut
Premature
polymer-
ization of the
material in the
cartridge due
to incident
light.
Contamination
of the material.
•Acoustic
signal (Close
hood)
•Tinted
window
•Protection
against
damage to
the printer
•Protectionof
the material
2Build
platform
Creation of
the printed
objects
Mechanical
hazards by the
build platform
falling down
•Construction-
safe design
•Fixation lever
Protection
against
crushing
Leaking,
slopping over
material due to
the build
platform
falling down
into the filled
cartridge.
•Protection
against
health
impairments
•Protection
against
environ-
mental
damage

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3 Cartridge Material
supply for
print jobs
Leaking,
slopping over
materialduring
transport of
the cartridge.
Dripping build
platform
•Handleat the
bottom
section, not
the top
section
•Accidental
swivelling
impeded by
the handle at
the bottom
section
•Protection
against
health
impairments
•Protection
against
environ-
mental
damage
Wrap around
rim at the top
edge
4Material
bottle
Material
supply for
print jobs
Leaking,
slopping over
materialduring
transport,
opening or
handling of the
bottle
•Robust
design of the
material
bottle
•Material
bottle can be
held stable
and does not
give in to
pressure
•Protection
against
health
impairments
•Protection
against
environ-
mental
damage
No.
Working
area Tasks / Work Type of hazard
Safety
equipment
Protective
effect

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2.7 Safety instructions for potential hazard areas
2.7.1 Electromagnetic waves
Even though the valid standards are observed, it is possible that the device reacts to radio
frequency interference or the operation of other devices in the immediate vicinity.
Do not operate devices that generate electromagnetic waves in the same room as this
device.
Take appropriate measures in the case of radio interference, e.g. a new orientation, a new
device position or electromagnetic shielding.
Only use the original accessories recommended and supplied by the manufacturer. Failure
to do so can result in increased interference emissions or decreased immunity of the
device.
2.7.2 Mechanics
Whilst the device is in operation, there are the following risks in the build chamber:
•Risk of crushing
•Risk of damage to the device
To prevent injury to the user inside the device, never remove the housing cover and do not
open the hood by force while the device is in operation.
Do not use the device when the hood is damaged (cracks, holes, missing window etc.).
2.7.3 Electrical safety
If covers are opened or parts are removed which are only accessible with tools, voltage-
carrying components may be exposed. The plugs may also be under voltage. There is a risk of
electric shock.
Electrical work must only be carried out by your authorized service partner.
Before connecting the device, check that the supply voltage and frequency are correct at
the point of installation (see electrical data and the information on the type plate in the
Operating Instructions, “Document of equal applicability and required files”, page 7).
To avoid injury to the user and for cooling reasons and fire protection, never remove the
housing covers.
For installation, observe the requirements of the manufacturer for house installation.
To prevent the risk of electric shock, connect the device only to a power supply with a
protective conductor.
The mains plug is used as a supply circuit disconnecting means. Always connect the mains
plug to an easily accessible protective contact socket.
Connect the grounded and freely accessible protective contact socket to a separately
secured circuit.
Make sure that the protective contact socket is equipped with a residual current circuit
breaker (FI).

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Connect the printer to a separately secured circuit or make sure that no devices are
connected that cause severe supply voltage fluctuations when switched on. These
fluctuations interfere with the electronic controls and may cause failure of the system.
Disconnect power before cleaning and maintenance work approved to be performed by
the user.
If you need to disconnect the unit from the power supply at a later time: Disconnect the
plug from the protective-contact mains socket, not on the device.
2.7.4 Hazardous materials
Incorrect handling of the device, the accessories or non-compliance with the processes
described in these Operating Instructions may lead to contact of the user with unpolymerized
material. This may result in health damage, e. g. skin irritations.
Depending on the material, there is a risk of skin irritations, allergic reactions or respiratory
diseases without the corresponding safety precautions.
Observe the Instructions for Use of the materials used (“Document of equal applicability
and required files”, page 7).
Wear protective gear (“Personal protective equipment”, page 11).
Make sure that the room is sufficiently ventilated when working with the materials or
handling the material bottles.

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2.8 Safety information for the individual operating phases
2.8.1 Transport
Transport the device only as described in the Operating Instructions (see requirements
regarding transport and setting up in the Operating Instructions, “Document of equal
applicability and required files”, page 7).
In order to avoid corrosion on the device and subsequent damage to the device, transport
and store device only in the permissible temperature range and ambient conditions (see
requirements regarding the ambient conditions in the Operating Instructions, “Document
of equal applicability and required files”, page 7).
2.8.2 Initial operation
Ensure that this device is only operated by authorized and trained specialists.
If the device has been stored in a cold environment or at high humidity, maintain a drying
or temperature adjustment time of approx. 4 hours (without voltage) at room
temperature before initial operation.
Before connecting the device, check that the supply voltage and frequency are correct at
the point of installation (see electrical data in the Operating Instructions, “Document of
equal applicability and required files”, page 7).
The requirements regarding the location site and ambient conditions must be observed
(see requirements regarding the location site and ambient conditions in the Operating
Instructions, “Document of equal applicability and required files”, page 7).
2.8.3 Operation
The device may only be operated by authorized and trained technical personnel.
Keep unauthorized persons, such as patients, children and animals, away from the device.
In all cases of doubt regarding the safety of the appliance, switch off the appliance and
take suitable measures to prevent further use.
Prior to connecting power or operation, check the device, the accessories and protective
equipment for any damage.
Do not use damaged, non-functioning equipment or accessories; instead notify your
authorized service partner.
In order to ensure the product safety and warranty services, the device must be exclusively
operated with the original accessories from Ivoclar Vivadent, particularly the original
power cord. The user bears the risk when using non-approved accessories.
To ensure process reliability, Ivoclar Vivadent recommends using only approved materials.
Never bypass the safety equipment of the device or set it out of operation (“Working
areas, potential hazards and safety measures on the device”, page 12).
Operate the device only with the build chamber closed.

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To prevent damage to the device and a reduction of the device performance, observe the
cleaning requirements and cycles (see “Cleaning by the user”, page 18 in these Short
Instructions as well as the overview and instructions for the cleaning and maintenance
work in the Operating Instructions, “Document of equal applicability and required files”,
page 7).
Only operate the device unsupervised if the operating conditions for unsupervised
operation described below are fulfilled.
Unsupervised operation:
The device may be operated unsupervised, provided the national and local laws and provisions
allow for such action and provided that they are observed. Furthermore, the requirements of
the respective insurance company must be met.
Never use the device if the build chamber is heavily soiled.
Protect the device against unauthorized access.
2.8.4 Cleaning by the user
Only clean as specified in these Operating Instructions and observe the related safety
regulations (see overview and requirements regarding cleaning and maintenance work in
the Operating Instructions, “Document of equal applicability and required files”, page 7).
2.8.5 Improper maintenance, modifications and repairs
Improper service and improper repairs or modifications will endanger patients and users and
result in damage to the device and the final products.
Should you carry out any repairs or maintenance of the device or modifications or remove the
housing without prior written consent by an authorized service partner, all warranty claims
are void.
Unauthorized opening and removal of components can expose voltage-carrying components.
The plugs may also be under voltage. There is a risk of electric shock!
Maintenance as well as repairs of damaged safety equipment or machine parts must only
be carried out by a service partner authorized by Ivoclar Vivadent.

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3 Additional information
•Download link Operating Instructions PrograPrint System:
https://www.ivoclardigital.com/prograprint-manual
•Download link PrograPrint Manager:
https://www.ivoclardigital.com/prograprint-manager
•Download link Test File:
https://www.ivoclardigital.com/prograprint-testfile
•Download link software required for PrograPrint:
https://www.ivoclarvivadent.com/en/cad-cam-download-center/
Ivoclar Vivadent AG herewith confirms that the radio equipment of PrograPrint PR5 (dental
laboratory device) complies with the directive 2014/53/EEC. The entire text of the EU
Declaration of Conformity can be found under the following link:
https://www.ivoclardigital.com/prograprint

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