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Test Number : E20-593
Test Name : Backup and Recovery Implementation
Vendor Name : EMC
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E20-593 test Format | E20-593 Course Contents | E20-593 Course Outline | E20-593 test Syllabus | E20-593 test Objectives

Exam Title : Dell EMC Certified Specialist - Implementation Engineer - NetWorker (DECS-IE)
Exam ID : E20-593
Exam Duration : 90 mins
Questions in test : 60
Passing Score : 63%
Exam Center : Pearson VUE
Real Questions : Dell EMC NetWorker Specialist Real Questions
VCE VCE test : Dell EMC E20-593 Certification VCE Practice Test

Dell EMC NetWorker Overview 10%
- Describe a NetWorker solution and its advantages
- Identify and describe the NetWorker software components and their roles, data protection functions, and terminology
- Explain the use of NetWorker control data and administrative interfaces

Dell EMC NetWorker Modules Overview 15%
- Explain how NetWorker modules work with native applications to support backup and recovery
- Explain the backup and recovery process with NetWorker modules
- Explain the functionality of various NetWorker modules; for example, NMM and NMDA

Dell EMC NetWorker Installation and Configuration 40%
- Describe the NetWorker architecture and components, including processes and backup data flow
- Identify and describe how NetWorker and NetWorker Management Console are installed and licensed
- Identify and describe how to configure NetWorker backups; including client, protection group, policy and directive resources, and client save set and backup command attributes
- Explain the NetWorker backup options; including synthetic full backup, block based backup, snapshot management, and VMware backup options
- Identify and describe the features of NetWorker backup devices and how they are configured and managed; including device types, media pools, client direct backups, cloning, and staging

Dell EMC NetWorker Administration and Management 25%
- Identify and describe the NetWorker security features; including NetWorker authentication (AuthC), NetWorker user groups, logs, and configuring firewalls
- Identify and describe how the NetWorker server and NetWorker Management Console are configured and managed; for example: notifications, reports, parallelism, multi-tenancy
- Identify and describe how to recover Windows hosts and configure NetWorker in cluster environments
- Identify and describe how NetWorker recoveries are performed; for example: directed, browsable, and save set
- Describe the management and backup and recovery of NetWorker databases; for example: media and resource databases and client file indexes

Dell EMC NetWorker Cloud Enablement 10%
- Describe the NetWorker features and capabilities that support backup to and in the Cloud
- Describe how to "configure" NetWorker with CloudBoost and Cloud Tier
- Describe how to "manage" NetWorker with CloudBoost and Cloud Tier
- Describe the features and capabilities provide by the NetWorker vRealize Data Protection Extension

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EMC guide

the use of IEC 60601-1-2 for trying out clinical gadgets | E20-593 Practice Questions and Dumps

For advantageous EMC testing, clinical producers may still personalize a specifications doc such as IEC 60601-1-2.

as the electromagnetic spectrum becomes more and more congested and digital gadgets proliferate, making certain electromagnetic compatibility (EMC) among electrical and digital device turns into a crucial challenge.

ensuring EMC is a essential difficulty for agencies producing electrical and electronic scientific gadgets. These kinds of devices should function as intended and not intervene with different machine, or the effects could be catastrophic. For clinical producers, making bound that instruments meet EMC requirements is not only a advertising necessity, however also a societal situation.

There are a couple of EMC requisites, however none of them alone will supply applicable testing instructions for enormously really good clinical contraptions. To cut back confusion and ensure that devices could be Checked correctly, clinical manufacturers should still use an present general as a e book for constructing a customised checking out plan.

IEC 60601-1-2

The overseas Electrotechnical commission (IEC) is a worldwide body that promotes international standardization in electronics. In 1993 it released the 60601-1-2 common, "medical Electrical gadget—half 1: ordinary requirements for security, modification No. 2. Collateral common: Electromagnetic Compatibility requirements and tests."1

The IEC 60601 average offers an effective basis for medical gadget testing. besides the fact that children they're incredibly new, the IEC 60601-1-2 necessities have right away turn into diagnosed during the area and are instrumental in testing to the eu clinical contraptions Directive. agencies such as the American countrywide requisites Institute (ANSI) use the IEC 60601 usual as a groundwork for his or her personal necessities.

This doc specifies ideal tiers for immunity and refers to different files to specify emission degrees. despite the fact, these ranges might also no longer be strict ample to be sure that device will operate as intended. producers should still use the IEC standards as a e book but tailor them to produce product-selected limits.

verify standards and limits

The IEC 60601-1-2 commonplace specifies examine limits for emissions, immunity, electrostatic discharge (ESD), radiated radio-frequency electromagnetic fields, bursts, and surges.

Emissions. device may still comply with the performed and radiated emissions requirements of the foreign particular Committee on Radio Interference (CISPR). Classification of equipment for this goal is based on supposed use and determined by way of the brand.

gadget may be Checked for emissions at a typical check site, which might include a turntable and floor plane, and have favourite attenuation curves. gadget might also even be tested after it has been installed on the clients' premises. it's recognized that medical equipment may also have wonderful setting up concerns and that category checking out of the setting up is the handiest purposeful solu-tion to demonstrate compliance to the requirements.

producers should seek advice from CISPR eleven for the acceptable necessities and amplitude degrees once the type of device and test area has been decided.2

currently, there are not any necessities for low-frequency emissions, harmonic distortion, and voltage fluctuations, however some machine that function in an intermittent mode will need to meet certain diversifications of the CISPR 14 click requirements.three

CISPR 11 covers a frequency latitude from a hundred and fifty kHz to 18 GHz. performed emissions for low- and medium-voltage vigor mains (100–415 V) are carried out from one hundred fifty kHz to 30 MHz. The frequency range for radiated emissions is from one hundred fifty kHz to 18 GHz. reckoning on the class and use of the machine, a considerable number of frequency stages may be described. simplest the magnetic component of the radiated box is measured from one hundred fifty kHz to 30 MHz. Above 30 MHz, each the vertical and horizontal components of the container must be measured.

Amplitude limits in regular are established to give protection to the public broadcast functions, not for device that might also must function in close proximity to sensitive clinical gadget.

The specification additionally refers to frequencies precise through the foreign Telecommunication Union: 2450 MHz for industrial, 5800 MHz for scientific, and 24,a hundred twenty five MHz for clinical device.

Immunity. generic immunity necessities are designated in IEC 60601-1-2. test tiers are given and examine strategies are in response to the IEC 801 sequence of immunity necessities. If lower limits are justified, accompanying files should clarify this and describe any motion that will, as a final result, be taken with the aid of the installer or person.

Accompanying documents should still encompass instructions for averting or picking out and resolving antagonistic electromagnetic results. If the use of the gadget is restricted as a result of its electromagnetic features, valuable restrictions should still be described within the accompanying documents.

Compliance with the requirements should be checked by way of verifying that the device continues to function its intended features as precise by the company or fails without creating a security hazard.

ESD. machine should conform to the present edition of IEC 801-2.four A restrict of 3 kV applies for direct contact discharge to all conductive attainable parts and coupling planes. A restrict of 8 kV applies for air discharge to nonconductive purchasable constituents.

Radiated Radio-frequency Electromagnetic Fields. gadget should conform to the IEC 801-three necessities, which might be being up-to-date.5 A restrict of 3 V/m should be used over a frequency range of 26 MHz to 1 GHz. other tiers practice to gadget utilized in shielded locations, equivalent to x-ray and MRI amenities. The three-V/m requirement is reduced in proportion to the expanding shielding effectiveness of the region.

There are provisions for amplitude modulation of the signal, based upon the passband of the gadget under verify (EUT). If the EUT does not have a passband, the sign should be amplitude modulated at 1 kHz.

Bursts. verify methods and instruments specific in IEC 801-4 may still be followed.6 A 1-kV stage applies to device linked to the energy line with a plug. For completely put in equipment, a degree of two kV applies. Interconnecting strains longer than three m may still be able to stand up to a 0.5-kV surge.

Surges. examine methods and gadgets distinctive in IEC 801-5, which is at present still below consideration, may still be followed.7 power strains may still meet degrees of 1 kV for differential mode and 2 kV for usual mode. sign lines don't need to be established, and telecom strains are lined via other standards. Ring wave and damped sinusoid checks don't seem to be applicable.

There are future provisions for voltage dips, brief interruptions, and voltage variations on energy lines, as well as for conducted immunity above 9 kHz and magnetic container immunity.

custom standards

producers of electrical and digital device for any use are recognizing the want for standards that be sure compatibility amongst equipment. scientific electronics manufacturersalso recognize that such regularly occurring standards are not always appropriate; they could be too severe, or, even worse, now not extreme sufficient to offer protection to their products. To decrease confusion and to make sure that check necessities can be applicable, clinical producers may still use an existing doc akin to IEC 60601-1-2 as a groundwork for creating their own product-selected specifications.


1. "scientific Electrical gadget part 1: ordinary requirements for safeguard, amendment No. 2. Collateral normal: Electromagnetic Compatibility—requirements and exams," Geneva, IEC, Bureau crucial de la commission Electrotechnique, 1st ed, 1993.

2. international particular Committee on Radio Interference, CISPR book 11, "Limits and techniques of dimension of Radio Interference characteristics of business, Scientific and scientific (ISM) Radio Frequency device (aside from Surgical Diathermy equipment)," Geneva, IEC, 2nd ed, 1990.

3. international special Committee on Radio Interference, CISPR publication 14, "Limits and methods of Measurements of Radio Interference characteristics of household Electrical appliances, moveable tools and identical Electrical equipment," Geneva, IEC, 2nd ed, 1985.

four. IEC 801-2, "Electromagnetic Compatibility for Industrial-method size and manage device, part 2: Electrostatic Discharge requirements," Geneva, IEC, 2nd ed, 1991.

5. IEC 801-three, "Electromagnetic Compatibility for Industrial-technique measurement and handle gadget, part three: Radiated Electromagnetic field requirements," Geneva, IEC, 1st ed, 1984, third affect, 1991.

6. IEC 801-4, "Electromagnetic Compatibility for Industrial-procedure dimension and manage equipment, half four: Electrical speedy Transient/Burst necessities," Geneva, IEC, 1st ed, 1988.

7. IEC 801-5, "Electromagnetic Compatibility for Industrial-technique size and manage gadget, part 5: Surge Immunity requirements," draft, Geneva, IEC, July 1992.

Gary Fenical is a senior EMC engineer with Instrument Specialties business, Inc. (Delaware Water gap, PA).

Illustration with the aid of Sarah Whitehead

Copyright ©1998 medical device & Diagnostic business

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