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EMC E20-562 : VPLEX Specialist test for Storage Administrators Exam

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Test Number : E20-562
Test Name : VPLEX Specialist test for Storage Administrators
Vendor Name : EMC
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E20-562 test Format | E20-562 Course Contents | E20-562 Course Outline | E20-562 test Syllabus | E20-562 test Objectives


Exam Title : Dell EMC Certified Specialist - Systems Administrator - VPLEX (DECS-SA)
Exam ID : E20-562
Exam Duration : 90 mins
Questions in test : 60
Passing Score : 63%
Official Training : VPLEX Management (MR-1CN-VPLEXMGMT)
Exam Center : Pearson VUE
Real Questions : Dell EMC VPLEX Specialist Real Questions
VCE VCE exam : Dell EMC E20-562 Certification VCE Practice Test

VPLEX Concepts 25%
- VPLEX terminology and configurations
- VPLEX product hardware and software architecture
- VPLEX application of VS2 and VS6 technology and upgrading from VS2 to VS6
- VPLEX I/O Operations

VPLEX Storage Provisioning 35%
- Virtual Volume Provisioning
- Integrating VPLEX into an existing environment and encapsulating storage
- Creating VPLEX Distributed Devices
- Device and extent management on VPLEX devices

Volume Management and Protection 25%
- Expanding VPLEX devices
- Performing data migration using VPLEX
- Protecting VPLEX with RecoverPoint

VPLEX Monitoring 15%
- VPLEX events and system reports to an ESRS Gateway
- SNMP data collection
- Setup performance monitors in VPLEX
- Analyze monitoring data in VPLEX



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EMC guide

using IEC 60601-1-2 for trying out clinical gadgets | E20-562 Latest subjects and Test Prep

For helpful EMC testing, medical manufacturers should customize a requisites doc such as IEC 60601-1-2.

because the electromagnetic spectrum becomes increasingly congested and digital contraptions proliferate, guaranteeing electromagnetic compatibility (EMC) among electrical and electronic device becomes a essential problem.

making certain EMC is a a must have concern for businesses producing electrical and electronic medical devices. These types of devices ought to function as intended and not intrude with different gadget, or the effects may well be catastrophic. For medical producers, making sure that instruments meet EMC standards isn't only a advertising necessity, however additionally a societal concern.

There are a few EMC requirements, but none of them on my own will provide appropriate trying out guidelines for totally really expert medical contraptions. To reduce confusion and confirm that gadgets should be Tested appropriately, scientific manufacturers should use an current usual as a e book for constructing a customised testing plan.

IEC 60601-1-2

The foreign Electrotechnical commission (IEC) is a worldwide physique that promotes international standardization in electronics. In 1993 it released the 60601-1-2 typical, "scientific Electrical machine—part 1: commonplace necessities for security, modification No. 2. Collateral usual: Electromagnetic Compatibility requirements and checks."1

The IEC 60601 usual presents a solid groundwork for clinical equipment testing. however they're extraordinarily new, the IEC 60601-1-2 requirements have without delay turn into diagnosed right through the area and are instrumental in testing to the eu clinical devices Directive. organizations such because the American national requisites Institute (ANSI) use the IEC 60601 commonplace as a groundwork for his or her own necessities.

This document specifies ideal levels for immunity and refers to other files to specify emission stages. despite the fact, these tiers might also no longer be strict ample to make sure that device will operate as intended. producers should use the IEC necessities as a ebook but tailor them to produce product-selected limits.

examine necessities and boundaries

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

Emissions. device should agree to the carried out and radiated emissions requirements of the international particular Committee on Radio Interference (CISPR). Classification of machine for this purpose is in keeping with supposed use and determined by means of the manufacturer.

equipment may well be demonstrated for emissions at a common verify web page, which would include a turntable and floor airplane, and have regularly occurring attenuation curves. machine may also be Tested after it has been installed on the clients' premises. it is recognized that scientific equipment might also have interesting installing considerations and that category checking out of the setting up is the best practical solu-tion to show compliance to the necessities.

manufacturers may still discuss with CISPR 11 for the acceptable requirements and amplitude ranges once the type of equipment and check region has been decided.2

currently, there are not any requirements for low-frequency emissions, harmonic distortion, and voltage fluctuations, however some machine that function in an intermittent mode will should meet certain diversifications of the CISPR 14 click on necessities.3

CISPR 11 covers a frequency latitude from one hundred fifty kHz to 18 GHz. performed emissions for low- and medium-voltage power mains (100–415 V) are carried out from a hundred and fifty kHz to 30 MHz. The frequency latitude for radiated emissions is from a hundred and fifty kHz to 18 GHz. depending on the class and use of the device, various frequency tiers may well be defined. most effective the magnetic component of the radiated container is measured from a hundred and fifty kHz to 30 MHz. Above 30 MHz, each the vertical and horizontal components of the field have to be measured.

Amplitude limits in conventional are based to protect the general public broadcast functions, not for machine that might also should operate in shut proximity to sensitive clinical machine.

The specification additionally refers to frequencies unique by the foreign Telecommunication Union: 2450 MHz for industrial, 5800 MHz for scientific, and 24,125 MHz for medical gadget.

Immunity. universal immunity necessities are certain in IEC 60601-1-2. look at various degrees are given and examine strategies are in accordance with the IEC 801 series of immunity requirements. If lower limits are justified, accompanying documents should clarify this and describe any action on the way to, as a end result, be taken by means of the installer or consumer.

Accompanying documents should still include instructions for avoiding or opting for and resolving hostile electromagnetic consequences. If using the machine is limited on account of its electromagnetic qualities, significant restrictions may still be described within the accompanying files.

Compliance with the requirements should be checked via verifying that the gadget continues to perform its meant functions as precise by the company or fails without growing a safety hazard.

ESD. equipment may still conform to the latest edition of IEC 801-2.four A restrict of 3 kV applies for direct contact discharge to all conductive attainable elements and coupling planes. A restrict of 8 kV applies for air discharge to nonconductive purchasable materials.

Radiated Radio-frequency Electromagnetic Fields. device should conform to the IEC 801-three requirements, that are 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 stages follow to gadget utilized in shielded areas, such as x-ray and MRI facilities. The three-V/m requirement is diminished in proportion to the expanding protecting effectiveness of the region.

There are provisions for amplitude modulation of the signal, depending upon the passband of the device under examine (EUT). If the EUT doesn't have a passband, the sign should be amplitude modulated at 1 kHz.

Bursts. verify strategies and gadgets precise in IEC 801-4 should still be followed.6 A 1-kV level applies to gadget connected to the power line with a plug. For permanently installed device, a degree of two kV applies. Interconnecting lines longer than 3 m should be capable of stand up to a 0.5-kV surge.

Surges. verify strategies and instruments precise in IEC 801-5, which is currently nonetheless under consideration, may still be adopted.7 energy strains should still meet ranges of 1 kV for differential mode and a couple of kV for regular mode. sign traces don't need to be demonstrated, and telecom lines are coated via different necessities. Ring wave and damped sinusoid assessments don't seem to be applicable.

There are future provisions for voltage dips, brief interruptions, and voltage variations on vigor lines, in addition to for performed immunity above 9 kHz and magnetic field immunity.

custom necessities

manufacturers of electrical and digital device for any use are recognizing the need for standards that ensure compatibility among device. medical electronics manufacturersalso admire that such everyday requirements are not necessarily applicable; they may be too severe, or, even worse, no longer extreme adequate to supply protection to their products. To diminish confusion and to make sure that examine specifications may be acceptable, clinical producers may still use an present document akin to IEC 60601-1-2 as a foundation for developing their own product-selected necessities.

REFERENCES

1. "scientific Electrical gadget part 1: general necessities for protection, modification No. 2. Collateral average: Electromagnetic Compatibility—necessities and checks," Geneva, IEC, Bureau significant de la fee Electrotechnique, 1st ed, 1993.

2. foreign particular Committee on Radio Interference, CISPR book 11, "Limits and methods of dimension of Radio Interference qualities of commercial, Scientific and clinical (ISM) Radio Frequency device (with the exception of Surgical Diathermy equipment)," Geneva, IEC, 2nd ed, 1990.

3. overseas special Committee on Radio Interference, CISPR booklet 14, "Limits and techniques of Measurements of Radio Interference characteristics of household Electrical appliances, moveable tools and equivalent Electrical equipment," Geneva, IEC, 2nd ed, 1985.

four. IEC 801-2, "Electromagnetic Compatibility for Industrial-process size and control machine, part 2: Electrostatic Discharge requirements," Geneva, IEC, 2nd ed, 1991.

5. IEC 801-3, "Electromagnetic Compatibility for Industrial-method dimension and manage device, part 3: Radiated Electromagnetic box necessities," Geneva, IEC, 1st ed, 1984, 3rd affect, 1991.

6. IEC 801-four, "Electromagnetic Compatibility for Industrial-technique measurement and handle machine, half 4: Electrical speedy Transient/Burst requirements," Geneva, IEC, 1st ed, 1988.

7. IEC 801-5, "Electromagnetic Compatibility for Industrial-technique dimension and handle gadget, half 5: Surge Immunity necessities," draft, Geneva, IEC, July 1992.

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

Illustration through Sarah Whitehead

Copyright ©1998 scientific gadget & Diagnostic business


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