Codonics Virtua E User manual

Table of Contents
EN - English .................................................................................................................................... 21
Documentation Notice .............................................................................................................. 21
Overview.................................................................................................................................... 21
Specifications............................................................................................................................. 21
Product Information.................................................................................................................. 22
Warnings and Limitations of Use .............................................................................................. 22
Location of Safety and Compliance Labels............................................................................ 22
Voltage Warning.................................................................................................................... 24
Laser Warning........................................................................................................................ 25
Compliance............................................................................................................................ 25
Serial Number, Configuration, Date Code, and Modification Codes..................................... 25
ESD Caution ........................................................................................................................... 26
Potential for Radio Frequency Interference on Device Operation........................................ 26
Potential for Radio and Television Interference ................................................................... 27
Guidance Regarding Electromagnetic Emissions and Immunity........................................... 27
Safety Precautions................................................................................................................. 29
Location Precautions ............................................................................................................. 30
Cleaning Precautions............................................................................................................. 31
Media Precautions................................................................................................................. 31
Codonics Virtua Medical Image Viewer................................................................................. 32
Medical and Patient Information .......................................................................................... 32
Disposal Requirements.......................................................................................................... 32
European Disposal Requirements ......................................................................................... 32
Indications for Use................................................................................................................. 33
Additional Warnings.............................................................................................................. 33
FR - Français................................................................................................................................... 35
Documentation Avis .................................................................................................................. 35
Aperçu ....................................................................................................................................... 35
Caractéristiques......................................................................................................................... 35
Produit Informations ................................................................................................................. 36
Mises en garde et Limites de Utilisation ................................................................................... 36
Lieu de Sécurité et Conformité Étiquettes............................................................................ 37
Tension Avertissement.......................................................................................................... 38

Ártalmatlanítás Követelmények.......................................................................................... 218
európai Ártalmatlanítás Követelmények............................................................................. 218
Jelzések mert Használat ...................................................................................................... 219
További Figyelmeztetések ................................................................................................... 219
IS - Íslenska................................................................................................................................... 221
Skjalagerð Takið eftir............................................................................................................... 221
Yfirlit ........................................................................................................................................ 221
Upplýsingar.............................................................................................................................. 221
Vara Upplýsingar ..................................................................................................................... 222
Viðvaranir og Takmarkanir af Notaðu ..................................................................................... 222
Staðsetning af Öryggi og Fylgni Merki................................................................................. 222
Spenna Viðvörun ................................................................................................................. 224
Leysir Viðvörun.................................................................................................................... 225
Fylgni.................................................................................................................................... 225
Rað Fjöldi, Stillingar, Dagsetning Kóða, og Breyting Kóðar ................................................. 225
ESD Varúð............................................................................................................................ 226
Möguleiki fyrir Útvarp Tíðni Truflun á Tæki Aðgerð............................................................ 226
Möguleiki fyrir Útvarp og Sjónvarp Truflun......................................................................... 227
Leiðbeiningar Varðandi Rafsegul Losun og Ónæmi............................................................. 227
Öryggi Varúðarráðstafanir................................................................................................... 229
Staðsetning Varúðarráðstafanir .......................................................................................... 230
Þrif Varúðarráðstafanir........................................................................................................ 230
Fjölmiðlar Varúðarráðstafanir............................................................................................. 231
Codonics Virtua Læknisfræðilegt Mynd Áhorfandi ............................................................. 231
Læknisfræðilegt og Sjúklingur Upplýsingar ......................................................................... 232
Förgun Kröfur ...................................................................................................................... 232
Evrópskt Förgun Kröfur ....................................................................................................... 232
Ábendingar fyrir Notaðu...................................................................................................... 233
Viðbót Viðvaranir................................................................................................................. 233
IT - Italiano ................................................................................................................................... 235
Documentazione Avviso.......................................................................................................... 235
Panoramica.............................................................................................................................. 235
Specifiche................................................................................................................................. 235
Prodotto Informazione............................................................................................................ 236
Avvertenze e Limitazioni di Uso .............................................................................................. 236

Posizione di Sicurezza e Conformità Etichette .................................................................... 237
Voltaggio avvertimento....................................................................................................... 238
Laser avvertimento.............................................................................................................. 239
Conformità........................................................................................................................... 239
Seriale Numero, Configurazione, Data Codice, e Modifica Codici ...................................... 239
ESD Attenzione.................................................................................................................... 240
Potenziale per Radio Frequenza Interferenza su Dispositivo Operazione .......................... 241
Potenziale per Radio e Televisione Interferenza................................................................. 241
Guida Per quanto riguarda Elettromagnetico Emissioni e Immunità ................................. 241
Sicurezza Precauzioni .......................................................................................................... 243
Posizione Precauzioni.......................................................................................................... 244
Pulizia Precauzioni............................................................................................................... 245
Media Precauzioni............................................................................................................... 245
Codonics Virtua Medico Immagine Spettatore ................................................................... 246
Medico e Paziente Informazione......................................................................................... 246
Disposizione Requisiti.......................................................................................................... 246
europeo Disposizione Requisiti ........................................................................................... 246
Indicazioni per Uso .............................................................................................................. 247
Aggiuntivo Avvertenze ........................................................................................................ 247
LT - lietuvių kalba......................................................................................................................... 249
Dokumentacija Pastebėti ........................................................................................................ 249
Apžvalga................................................................................................................................... 249
Specifikacijos ........................................................................................................................... 249
Produktas Informacija ............................................................................................................. 250
Įspėjimai ir Apribojimai apie Naudokite.................................................................................. 250
Vieta apie Saugumas ir Laikymasis Etiketės ........................................................................ 251
Įtampa Įspėjimas ................................................................................................................. 252
Lazeris Įspėjimas.................................................................................................................. 253
Laikymasis............................................................................................................................ 253
Serijinis Skaičius, Konfigūracija, Data Kodas, ir Modifikacija Kodai..................................... 253
ESD Atsargiai........................................................................................................................ 254
Potencialus dėl Radijas Dažnis Kišimasis ant Įrenginys Operacija....................................... 254
Potencialus dėl Radijas ir Televizija Kišimasis...................................................................... 255
Nurodymai Apie Elektromagnetinis Emisijos ir Imunitetas................................................. 255
Saugumas Atsargumo priemonės........................................................................................ 257

Virtua® E and Virtua® C
Medical Disc Publisher
EN - English
Documentation Notice
Codonics Products are Class I products intended for use by Healthcare Professionals.
Products packaging and labeling, including Graphic User Interface (GUI) for operation are
Offered in English and meet MDR, Annex I, Chapter III, 23.4, taking account the training and the
knowledge of the potential user.
*Web information, Key Specifications, Intended Use, User manual Appendix, Quick Start Guide &
Setup IFU are available in simple translation Member State Languages; primary IFU are available
in English
Overview
Virtua E and Virtua C are the perfect, economical, easy to use, image distribution accessories for
any modality. Its compact design features an advanced processor for receiving and managing
studies, a robotic disc recorder and printer, and a user-friendly web interface. A table-top touch
screen is included with the Virtua E model only. The built-in printer produces brilliant, full-color
disc labels that include patient demographics and the facility's address and logo for marketing.
Customers can create their own custom labels or use Codonics disc label design service offered
exclusively to our customers.
Specifications
Media Input: One 20-disc input bin
Media Output: One 25-disc output bin
Optical Drive: One CD/ DVD drives
Recordable Formats: CD-R, DVD-R
Label Print Technology: Inkjet
Print Resolution: Up to 4800 dpi
Ink Cartridge: One tri-color cartridge
User Interface:
15" LCD touch screen (Virtua E only)
Remote web browser access using Internet Explorer®
Performance: Up to 25 CDs per hour, 10 DVDs per hour (based on a typical clinical study and
network configuration)

Processor: Intel®Celeron®G3900
Data Storage: 40 GB
Interface: 10/100Base-T/Gigabit Ethernet (RJ-45)
Network Protocols:
DICOM Store SCP
DICOM query/retrieve (optional)
HTTP Web Server (for remote control and configuration)
Smart Drive: USB flash drive for storing configuration data
Power: Universal Input: 100-240VAC, 50/60 Hz, 175VA (rated power)
Dimensions: 10.5“ (26.7 cm) H, 18.2“ (46.2 cm) W, 21.7“ (55.1 cm) L
Weight:
Virtua E: 43 lbs. (19.3kg.)
Virtua C: 32 lbs. (14.6kg.)
Regulatory:
Full medical device compliance including Class 2 FDA and Class I MDR 2017/745/EU (CE),
GMP/QSR, ISO 13485:2016/NS-EN ISO 13485:2016, Electrical Safety IEC 60601-1 Ed. 3.1 and
EMC/EMI: FCC Class B and IEC 60601-1-2: Ed. 4 for Professional Healthcare Facilities
Product Information
For technical assistance with the Virtua, call Codonics Technical Support at the following
number:
Phone: [phone]
Toll Free: 800.444.1198 (USA only)
Technical Support is available anytime. Technical Support is also available online via email
and the Codonics web site:
Email: [email protected]
Web Site: www.codonics.com
General product information can also be requested by sending email to:
Email: [email protected]om
Please include your postal mailing address and telephone number in the email message.
Basic product information is returned via email unless otherwise requested.
Warnings and Limitations of Use
Location of Safety and Compliance Labels

The following figures show the locations of the imager’s safety and compliance
labels.
Location of compliance label at top of Controller
Location of compliance label at rear of Recorder

Location of ESD labels and caution safety labels
Voltage Warning
The exclamation point within an equilateral triangle and person reading a manual symbol are
intended to alert the user to the presence of important operating and maintenance (servicing)
instructions in the literature accompanying this device.
NO USER-SERVICEABLE PARTS INSIDE. REFER SERVICING TO QUALIFIED SERVICE
PERSONNEL. REMOVAL OF LABELS, COVERS, OR ENCASEMENT FASTENERS VOIDS
THE WARRANTY.
WARNING Do not modify this equipment without authorization of the manufacturer
THIS APPARATUS MUST BE ELECTRICALLY GROUNDED.
TO PREVENT FIRE OR SHOCK HAZARD, DO NOT EXPOSE THIS IMAGER TO RAIN OR
MOISTURE.
WARNING The power cord plug is the main disconnect for the device. The power outlet
should be near the device and be easily accessible.
WARNING Remove the power cord plug from the power outlet to disconnect overall power to
the device.
WARNING Grounding reliability can be achieved only when this equipment is connected to
an equivalent receptacle marked “Hospital Only” (that is, “Hospital Grade”).
WARNING To avoid risk of electric shock, this equipment must only be connected to a supply
mains with protective earth.
WARNING Do not touch a patient while also accessing Virtua internal components that are
under the front cover.
EQUIPMENT IS NOT TO BE USED AS A COMPONENT OF A LIFE SUPPORT SYSTEM.
Life support devices or systems are devices or systems that support or sustain life, and

whose failure to perform can be reasonably expected to result in a significant injury or death
to a person. A critical component is any component of a life support device or system whose
failure to perform can be reasonably expected to cause the failure of the life support device or
system, or to affect its safety or effectiveness
Laser Warning
The Codonics Virtua Medical Disc Publisher contains a laser diode in the Recorder unit of a
class higher than 1. To ensure continued safety, do not remove any covers or attempt to gain
access to the inside of the product. Refer all servicing to qualified personnel. The following
label appears inside your unit:
CLASS 1 LASER PRODUCT LASER KLASSE 1
Compliance
The Compliance label for the Virtua-E and Virtua-C models, which is affixed to the top of the
Controller is shown below.
Compliance label for Virtua-C and Virtua-E models
Serial Number, Configuration, Date Code, and Modification Codes
The serial number label is placed onto the compliance label. Serial number labels are also
located at the front of the Recorder and Controller, behind the output bin.
The serial number label includes the following information:
•The serial number (SN), which uniquely identifies the unit.
•The configuration number (CN), which details the build configuration.
•The modifications codes, which are to the right of the CN number and are a series of 20
numbers. When any of these numbers are blocked out, that identifies a modification that
was made to the unit.

•The date code in YYYY-MM format below the factory date code symbol.
Serial number label
ESD Caution
Connections to other pieces of equipment are made at the rear of the Codonics Virtua E and
Virtua C Medical Disc Publisher. These connectors are marked with a precautionary ESD
warning symbol, as shown below. Do not touch any of the pins of these connectors. When
making connections to the device, it is best done while the device is plugged in but not
powered on. ESD may cause erratic behavior of the device when powered on. Should this
occur, power to the device may have to be cycled. It is recommended that all staff involved in
making connections to the device be aware of these ESD precautions.
ESD labels at rear of Controller
Potential for Radio Frequency Interference on Device Operation
Both portable and mobile RF communications equipment can affect medical electrical
equipment, including Virtua E and Virtua C. Keep such RF communications equipment out of
the immediate area.

Potential for Radio and Television Interference
Virtua E and Virtua C generate and uses radio frequency energy, and if not installed and
used properly, that is, in strict accordance with the manufacturer’s instructions, may cause
interference to radio and television reception. Do not change the Display refresh rate, which
is set for 75 Hz. The device has been type tested and found to comply with Class B emission
limits for a computing device in accordance with the specifications in Subpart J of Part 15 of
FCC Rules, which are designed to provide reasonable protection against such interference
when operating in a commercial environment. Operation of the equipment in a residential
area is likely to cause interference, in which case the user, at his own expense, will be
required to take whatever measures may be appropriate to correct the interference. If your
device does cause interference to radio or television reception, you are encouraged to try to
correct the interference by one or more of the following measures:
•Reorient the receiving antenna
•Relocate the device with respect to the receiver
If necessary, you should consult Codonics Technical Support or an experienced
radio/television technician for additional suggestions. You may find the following booklet
prepared by the Federal Communications Commission helpful: How to Identify and Resolve
Radio-TV Interference Problems. This booklet is available from the U.S. Government Printing
Office, Washington, D.C. 20402, Stock No. 004-000-00345-4.
This product is in conformity with the protection requirements of EC Council directive
89/336/EEC on the approximation of the laws of the Member States relating to
electromagnetic compatibility. This product satisfies the Class B limits of EN55011. A
declaration of conformity with the requirements of the Directive has been signed by the
Director of Quality Assurance and Regulatory Affairs.
Guidance Regarding Electromagnetic Emissions and Immunity
Suitable Environments:
•Virtua-C/E is intended for use in professional healthcare facility environments, including
hospitals and medical clinics.
•Virtua-C/E has not been evaluated for use near HF surgical equipment. If use near HF
surgical equipment is desired, the user is responsible for verifying proper operation of the
Virtua-C/E. If Virtua-C/E does not perform correctly in this environment, move the Virtua-
C/E farther from the source of the electromagnetic disturbance.
•Virtua-C/E has not been evaluated for use in emergency medical vehicles.
As a support device, Virtua-C/E does not provide essential performance.
WARNING Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is necessary, this
equipment and the other equipment should be observed to verify that they are operating
normally
WARNING Use of accessories, transducers and cables other than those specified or
provided by the manufacturer of this equipment could result in increased electromagnetic

emissions or decreased electromagnetic immunity of this equipment and result in improper
operation.
WARNING Portable RF communications equipment (including peripherals such as antenna
cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of
the Virtua, its cables, or accessories. Otherwise, degradation of the performance of this
equipment could result.
Electromagnetic Emissions Standards and Test Levels:
Electromagnetic Immunity Standards and Test Levels:

Safety Precautions
•Never connect this device to any outlet or power supply that has a voltage or frequency
different than that specified and set on the rear of the device.
•When servicing the device, always power it off by pressing the System power button,
then unplug the device.
•Damage to the power cord may cause fire or shock hazard. When unplugging the power
cord, hold it by the plug only and remove the plug carefully.
•If the power cord needs to be replaced, replace it only with another Codonics power cord
manufactured specifically for your power configuration.

•If the device is smoking or making unusual sounds, power off and unplug the device
immediately.
•Do not insert foreign objects of any kind into the device; doing so can constitute a safety
hazard and cause extensive damage.
•Do not place any liquid containers on the device. If, for some reason, liquid seeps into the
device, power off the device and unplug the power cord from the source outlet. If used
without corrective measures, the device may be damaged.
•Do not use the device near flammable gases.
•Connect only Codonics-approved devices.
Location Precautions
•The device’s operating ambient temperature range is 15–30ºC (59–86ºF), with a relative
humidity of 20%–80%.
•If the device is moved quickly from an extremely cold place to a warmer one,
condensation is likely to form. Do not use the device if condensation has formed. Wait
until the condensation has evaporated. You can speed up the evaporation time by
moving the device to a drier location.
•Ventilation slots and holes are provided on the sides and rear of the device. Place the
device on a level, stable surface and locate it at least 10 cm (4 in.) from walls to ensure
proper ventilation.
WARNING: Adequate ventilation is required for proper operation of the device.
•Do not place device in a high humidity or high dust area. Airborne dirt particles can cause
interference with the operation of the device. Avoid placing the device in areas where
ventilation ducts, open doors, or frequent passers-by might expose the device and media
to high levels of debris.
•Do not locate the device in hot-springs areas where hydrogen sulfide and acidic ions are
likely to be generated.
•Do not locate the device where there are oily fumes and vapors.
•Do not locate the device in direct sunlight.
•Do not locate device near sources of high RF energy.
•Do not locate the device where it might be subject to jarring or vibrations, such as a table
or desk in a high-traffic area. Jarring and vibrations can affect the recording and labeling
of discs.

Cleaning Precautions
•Many plastic components are used in the device’s construction. Coat flecking and
deformation is likely to occur if the device is wiped with chemical dusters, benzene,
thinners, insecticides, or other solvents. Rubber and PVC materials left in contact with the
device for extended times will cause damage. Never use petroleum-based solutions or
abrasive cleaners.
•To clean the device cover, first power off the device by pressing the System power button
on the Controller front panel, then unplug the device. Clean the cover with a soft cloth
slightly moistened with a mild soap and water solution. Allow the cover to completely dry
before operating the device again.
•To clean the Display’s touch screen, use a mild soap and water mixture. Always apply
the soap and water mixture to a clean cloth or towel first and then clean the screen.
Liquid applied directly to the Display could possibly leak inside the device and cause
damage.
•Do not use alcohol. The touch screen can be damaged if cleaned with alcohol.
Media Precautions
•Discs with the word “reject” or a reject icon printed on the label have failed to record
properly and should be destroyed or disposed of to ensure the confidentiality of patient
medical information.
•Unwanted discs should be destroyed or disposed of to ensure the confidentiality of
patient medical information.
•Only use Codonics-recommended discs to ensure compatibility with the recording and
labeling system of the device. Contact Codonics Customer Service for a current list of
recommended discs and suppliers.
•Only use Codonics-recommended ink cartridges to ensure proper operation of the device
and proper labeling of the disc. Contact Codonics Customer Service for a current list of
recommended ink cartridges and suppliers.
•Never refill ink cartridges as this can cause damage to the mechanism of the device and
cause improper labeling of discs.
•Recorded discs should be stored in protective cases or sleeves when not in use to
protect from scratches and contamination that can interfere with data retrieval and label
legibility.
•Do not subject recorded discs to prolonged exposure to sunlight, ultraviolet light, or
extreme heat as this can interfere with data retrieval and label legibility.

Codonics Virtua Medical Image Viewer
•The Codonics Virtua Medical Image Viewer is not intended for diagnostic use. The viewer
is provided for reference use only as a post-diagnostic tool.
•Image quality can vary greatly from system to system based on the age, quality, and
resolution of the display device (monitor or LCD display), graphics card, cabling, and
ambient light conditions.
Medical and Patient Information
•Virtua log files might contain patient information. Use caution when distributing log files.
•CD and DVD media are not intended to be used as the only method for archiving medical
information. An overall strategy for archiving medical information that includes CD or
DVD media must ensure that multiple copies of the information be stored at multiple
locations. Media quality, handling, and storage conditions are important factors that must
be considered.
Disposal Requirements
Disposal of this product and consumables shall be in accordance with all applicable laws and
regulations in effect at the locality at the time of disposal. For additional information, refer to
Appendix A of the User’s Manual, Hazardous Material Information.
European Disposal Requirements
Codonics imagers and electronic accessory devices are not to be discarded or recycled;
rather they are to be returned to the manufacturer. Contact Codonics directly or by the link
provided for the latest information concerning:
•Identification of the country specific Importer/Distributor/Producer
•Product return and treatment of our electronic products
Manufacturer: Codonics Incorporated
17991 Englewood Drive
Middleburg Heights, OH 44130 USA
Phone: [phone]
Fax: [phone]
Email: W[email protected]
www.codonics.com
Codonics imagers and electronic accessory devices bearing the following symbol are subject
to European Directive on Waste Electrical and Electronic Equipment (WEEE) 2002/96/EC,
amended by Directive 2003/108/EC. The EN 50419 symbol indicates separate collection and
return required.

EN 50419 symbol
Indications for Use
Virtua Series devices are intended for digital medical image communication, processing, and
storage. Functions include transfer, “viewing client on CD/DVD” provision, storage, archive,
recording, and labeling of CD/DVD media. When configured, the ability to re-direct all or part
of a radiographic study to Codonics Horizon Series Medical Hardcopy Dry Imagers (Pre-
market notification K021054) or other approved 892.2040 medical hardcopy imager/printer is
provided. Typical users of this system are trained professionals, including but not limited to
physicians, nurses, and technicians.
Additional Warnings
WARNING The shipping cartons are heavy. To avoid injury, use two people to unpack and
position the components.
WARNING When removing the Controller or Recorder, hold under the front and rear of the
device. Do not lift device by the foam packaging.
WARNING Before placing the Recorder on top of the Controller, make sure your fingers are
not under the Recorder to avoid pinching them.
WARNING The power cord plug is the main disconnect for the device. The power outlet
should be near the device and be easily accessible.
WARNING Remove the power cord plug from the power outlet to disconnect overall power to
the device.
WARNING Grounding reliability can be achieved only when the equipment is connected to an
equivalent receptacle marked “Hospital Only” (that is, “Hospital Grade”).
WARNING To avoid risk of electrical shock, this equipment must only be connected to a
supply main with protective earth.
WARNING Before powering on the unit, make sure that the Recorder’s pick arm is not
holding a disc. If it is, remove the disc.
WARNING Do not touch the copper area of the cartridge print head.
WARNING The SmartDrive must be inserted for the device to operate. If the SmartDrive is
not inserted, the device can boot up but will not be able to process jobs.
WARNING If the SmartDrive is removed improperly while a study is being processed, file
corruption could occur.
WARNING Discs that fail to record properly are either labeled with the word “Reject” or not
labeled at all. These discs should be destroyed to protect the confidentiality of patient data.
WARNING Deleting a job that is in-progress can result in a disc that is either labeled with the
word “Reject” or not labeled at all. These discs should be destroyed to protect the
confidentiality of patient data.

WARNING CD and DVD media are not intended to be used as the only method for archiving
medical information. An overall strategy for archiving medical information that includes CD
and DVD media must ensure that multiple copies of the information be stored at multiple
locations. Media quality, handling, and storage conditions are important factors that must be
considered.
WARNING Virtua log files might contain patient information. Use caution when distributing
log files.
WARNING Virtua E and Virtua C are medical devices that contains software validated for
proper operation only as configured from Codonics. Loading external software such as anti-
virus programs can result in unsafe or ineffective operation. Codonics strongly advises
against modification of the device or software in any way
WARNING Always power off the device and disconnect the device’s power cords before
cleaning. Resume operation only after the surfaces are completely dry.
WARNING Run the Robotic Arm Calibration utility only when requested by Codonics
Technical Support personnel.
WARNING Initiate a remote access connection to Codonics only when requested by
Codonics Technical Support personnel.
WARNING System logs do not have the same user interface appearance and behavior as
other screens. These logs should not be accessed unless requested by Codonics Technical
Support personnel.

Virtua® E and Virtua® C
Medical Disc Publisher
IT - Italiano
Documentazione Avviso
Codonics Prodotti siamo Classe io prodotti previsto per uso di Assistenza sanitaria Professionisti.
Prodotti confezione e etichettatura, Compreso Grafico Utente Interfaccia (GUI) per operazione
siamo
Offerto nel inglese e incontrare MDR, Allegato IO, Capitolo III, 23.4, prendendo account il
formazione e il conoscenza di il potenziale utente.
*Ragnatela informazione, Chiave Specifiche, Destinato Uso, Utente Manuale Appendice, Presto
Inizio Guida & Impostare SE TU siamo a disposizione nel semplice traduzione Membro Stato Le
lingue; primario SE TU siamo a disposizione nel inglese
Panoramica
Virtua E e Virtua C siamo il Perfetto, economico, facile per use, Immagine distribuzione Accessori
per qualunque modalità. Suo compatto design Caratteristiche un Avanzate processore per
ricezione e gestione studi, un robotica disco registratore e stampante, e un facile da usare
ragnatela interfaccia. UN da tavolo toccare schermo è incluso con il Virtua E modello solo. Il
incorporato stampante produce brillante, pieno di colori disco etichette quello includere paziente
dati demografici e il della struttura indirizzo e logo per marketing. Clienti può creare loro proprio
personalizzato etichette o uso Codonics disco etichetta design servizio offerto esclusivamente to
nostro clienti.
Specifiche
Media Ingresso: Uno 20 dischi ingresso bidone
Media Produzione: Uno 25 dischi produzione bidone
Ottico Guidare: Uno CD/ DVD unità
Registrabile Formati: CD-R, DVD-R
Etichetta Stampa Tecnologia: Getto d'inchiostro
Stampa Risoluzione: Su per 4800 dpi
Inchiostro Cartuccia: Uno tricolore cartuccia
Utente Interfaccia:
15 " LCD toccare schermo (Virtua E solo)
Remote ragnatela browser accesso utilizzando Internet Explorer®

Prestazione: Su per 25 CD per ora, 10 DVD per ora (basato su un tipico clinico studia e Rete
configurazione)
Processore: Intel®Celeron®G3900
Dati Conservazione: 40 GB
Interfaccia: 10 / 100Base-T / Gigabit Ethernet (RJ-45)
Rete Protocolli:
DVENGO Negozio SCP
DICOM interrogare / recuperare (opzionale)
HTTP ragnatela server (per a distanza controllo e configurazione)
Inteligente Guidare: USB veloce guidare per immagazzinamento configurazione dati
Energia: universale Ingresso: 100-240 V CA, 50/60 Hz, 175VA (nominale energia)
Dimensioni: 10.5 " (26.7 cm) H, 18,2 " (46.2 cm) W, 21,7 " (55.1 cm) L
Peso:
Virtua E: 43 lbs. (19.3kg.)
Virtua C: 32 lbs. (14,6 kg.)
Normativa:
Pieno medico dispositivo conformità Compreso Classe 2 FDA e Classe io MDR 2017/745 / UE
(CE), GMP / QSR, ISO 13485: 2016 / NS-EN ISO 13485: 2016, Elettrico Sicurezza IEC 60601-1
Ed. 3.1 e EMC / EMI: FCC Classe B e IEC 60601-1-2: Ed. 4 per Professionale Assistenza
sanitaria Strutture
Prodotto Informazione
Per tecnico assistenza con il Virtua, chiamata Codonics Tecnico Supporto a il a seguire
numero:
Telefono:+1.440.243.1198
Pedaggio Gratuito:800.444.1198 (STATI UNITI D'AMERICA solo)
Tecnico Supporto è a disposizione in qualsiasi momento. Tecnico Supporto è anche a
disposizione in linea attraverso e-mail e il Codonics ragnatela posto:
E-mail:[e-mail]
ragnatela Posto:www.codonics.com
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Avvertenze e Limitazioni di Uso

Posizione di Sicurezza e Conformità Etichette
Il a seguire figuraS spettacolo il posizioni di il imager's sicurezza e conformità
etichette.
Posizione di conformità etichetta a superiore di Controller
Posizione di conformità etichetta a posteriore di Registratore