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Test Number : E20-260
Test Name : VPLEX Specialist for Implementation Engineers
Vendor Name : EMC
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E20-260 exam Format | E20-260 Course Contents | E20-260 Course Outline | E20-260 exam Syllabus | E20-260 exam Objectives


Exam Title : Dell EMC Certified Specialist - Implementation Engineer - VPLEX (DECS-IE)
Exam ID : E20-260
Exam Duration : 90 mins
Questions in exam : 60
Passing Score : 63%
Official Training : VPLEX Fundamentals (MR-1WP-VPLEXFD)
Exam Center : Pearson VUE
Real Questions : Dell EMC VPLEX Specialist Real Questions
VCE practice questions : Dell EMC E20-260 Certification VCE Practice Test

VPLEX Concepts 13%
- 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 Installation and Setup 23%
- Site Installation Preparation
- Port Identification and Installation Utilities
- Provision storage to VPLEX back-end ports
- Installing VPLEX using EMC procedures
- Installing VPLEX Witness
VPLEX Storage Provisioning 20%
- 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 20%
- Expanding VPLEX devices
- Performing data migration using VPLEX
- Protecting VPLEX with RecoverPoint
VPLEX Monitoring 10%
- VPLEX events and system reports to an ESRS Gateway
- SNMP data collection
- Setup performance monitors in VPLEX
- Analyze monitoring data in VPLEX
VPLEX Upgrades and Troubleshooting 13%
- VPLEX Data collection processes
- Basic troubleshooting on various VPLEX elements
- Basic VPLEX maintenance
- Expanding a VPLEX topology



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EMC for Test Prep

realizing the brand new EMC typical for scientific instruments: What producers should recognize Now | E20-260 Free exam PDF and exam Questions

at the start posted MDDI August 2002

ELECTRONICS

figuring out the new EMC normal for scientific instruments: What producers need to know Now

meeting the new necessities set forth in the latest version of 60601-1-2 might prove difficult for OEMs.

Don Sherratt

In 1993, the international Electrotechnical fee (IEC) published the first version of 60601-1-2, the overseas electromagnetic compatibility (EMC) average for medical instruments. quickly after, the european Committee for Standardization (CENELEC) adopted it as a eu Norm (EN) regular—with only minor changes. it'll therefore come as no shock that IEC's existing revision of 60601-1-2, posted in September 2001, became adopted by way of CENELEC almost immediately thereafter and posted as EN 60601-1-2:2001 it will seem in the official Journal of the european neighborhood in August 2002.

IEC (EN) 60601-1-2:2001 is regarded an immense rewrite of the original and should have profound effects on compliance in regards to two critical ecu directives: the active Implantable scientific contraptions Directive (ninety/385/EEC) and the medical contraptions Directive (ninety three/forty two/EEC), as well as CB Scheme requirements and related standards. whereas the phaseout date of the 1993 EN common can be two years from now, producers that export their products globally—or who plan to—and need to remain aggressive should still automatically start constructing ideas to handle the brand new average's impact on product design and building.

To support producers prepare for this transition, this text addresses the most huge variations between the first and 2d variations of IEC 60601-1-2, and descriptions key steps to compliance.

tougher standards, larger limits

the most massive revisions to IEC 60601-1-2 consist of multiplied testing limits for electrostatic discharge (ESD), radiated radio-frequency (RF) immunity, surge immunity, and electrical quick transients (EFTs). There are also required assessments for performed RF immunity, magnetic container immunity, voltage dips, harmonic distortion, and voltage flicker. furthermore, the general carries greater-comprehensive move/fail criteria, which require that medical utility be maintained throughout immunity tests and that the manufacturer define ideal criteria of clinical utility.

Electrostatic Discharge. The standard outlined in IEC 60601-1-2:2001 for measuring ESD is IEC 61000-4-2. It defines the range of test ranges in terms of distinct environmental and installing situations and establishes the acceptable test techniques. The objective of the general is to establish a common reproducible groundwork for evaluating the efficiency of equipment when subjected to ESD. desk I compares the ancient ESD dimension limits to the new ones.

IEC 60601-1-2:1993

IEC 60601-1-2:2001

IEC 801-2

IEC 61000-4-2

±3 kV for conductive constituents

±8 kV for nonconductive elements

±2, four, and 6 kV for conductive constituents

±2, four, and 8 kV for nonconductive parts

table I. A comparison of ESD requirements between the historic and new requisites.

These new requirements will possible demand that insulation thicknesses and creepage and clearance distances be more suitable than before to prevent arcing through and monitoring over insulation. They could additionally require enclosure substances to own multiplied antistatic properties, or that equipment requirements distinctive in person manuals mandate higher relative humidity degrees for working environments.

Radiated RF Immunity. in the first version of the usual, RF immunity requirements have been described via IEC 801-three. in the up-to-date version, they're described by means of IEC 61000-4-3 and are outlined separately for all times-helping and non-life-supporting medical electrical equipment. The frequency range of the requirements has been widened and allows for for gadgets specified for use simplest in shielded areas. different noteworthy modifications include an intentional RF receivers' operation-mode exemption and a mandate that affected person-coupled gadget ought to meet the identical necessities as different gadget. desk II presents a assessment of the two requirements.

There are distinctive look at various strategies described within the new normal for measuring RRFI of different clinical electrical gadget; producers should discuss probably the most suitable strategies with technical consultants at their testing lab.

IEC 60601-1-2:1993

IEC 60601-1-2:2001

IEC 801-three

IEC 61000-four-three

three V/m at ISM frequencies from 26 MHz to 1 GHz with 80% AM for non-lifestyles-aid gadget

3 V/m from 26 MHz to 1 GHz with eighty% AM modulation for life-assist machine

three V/m at ISM frequencies from 80 MHz to 2.5 GHz with 80% AM for non-existence-aid machine

10 V/m from 80 MHz to 2.5 GHz with 80% AM modulation for life-support machine

table II. A comparison of RF immunity necessities between the old and new requisites.

Electrical fast Transients. IEC 801-4 determined the EFT immunity necessities and verify strategies in the outdated normal, nonetheless it will be replaced through IEC 61000-four-4 within the new edition. the brand new ordinary defines the examine voltage waveform, range of examine ranges, look at various device, test setup, and examine process, as outlined in table III. One excellent alternate is the lack of differentiation between permanently and temporarily put in device. There are also enormous ameliorations within the requirements for testing levels and repetition expense, and circulate-fail criteria are an awful lot tighter beneath the brand new typical.

producers should still even be conscious that the new ordinary requires that handheld machine or components of handheld gadget be established with a man-made hand to simulate the capacitive coupling effect of the operator, as particular in CISPR 16-1. The synthetic hand is connected to the floor reference aircraft right through the assessments. This requirement is new for medical electrical equipment and may outcomes in dielectric stresses on sign or patient cables carrying excessive-frequency or high-voltage alerts. To cut back the expertise for this occurrence, manufacturers should take into account the category of cables utilized in interconnecting leads and be aware that affected person leads may should be changed.

IEC 60601-1-2:1993

IEC 60601-1-2:2001

IEC 801-4

IEC 61000-4-4

±1kV for mains-plug-class gadget

±2kV for permanent gadget

±0.5 kV for signal traces

2.5-kHz repetition price

±2kV on power strains

±1kV for signal lines

5-kHz repetition rate

table III. A evaluation of EFT necessities between the historic and new requisites.

Surge Immunity. IEC 61000-four-5 is the new ordinary that specifies test ranges relating to distinct environmental and installing conditions. It establishes a standard reference for evaluating the efficiency of gadget when subjected to excessive-power disturbances on the power and interconnection lines, and specifies sweeping section angles over certain voltage levels. The determination of compliance is based on the response of the equipment, for the reason that each and every surge personally, and considering the outcomes of any coupling between cables that are proven without delay and people that don't seem to be. table IV items a assessment of the historical and the brand new necessities.

These new requirements might necessitate circuit redecorate and component alterations in medical instruments. while the higher voltage requirement remains the equal, the brand new decrease voltage requirement means multiple level of surge coverage can be essential and should must begin at ±0.5 kV.

New exams, strategies, and prerequisites

IEC 60601-1-2:1993

IEC 60601-1-2:2001

IEC 801-5

IEC 61000-four-5

±2kV standard mode

±1kV differential mode

±1.5, 1, and a pair of kV usual mode

±0.5 and 1 kV differential mode

desk IV. A comparison of surge immunity necessities between the historical and new requirements.

besides a major change in test limits, the new typical also specifies alterations in the classification of products and descriptions the strategies and new machine integral to examine emissions and immunity compliance.

Product Classification. the brand new general stipulates that nonmedical device used in a scientific device need most effective meet the applicable CISPR necessities—in most instances CISPR 14, 15, and 22. Most scientific electrical machine or techniques will continue to be subject to the requirements of CISPR 11 and have to be described as group 1 or 2 and class A or B. producers should still take into account that hospitals are sometimes considered residential or home; therefore, type B limits are sometimes imposed.

Harmonic Distortion. There are two new necessities for deciding on emissions compliance. the primary, IEC 61000-three-2, Limits for harmonic existing emissions, addresses the impact on the sinusoidal waveform of the main deliver of products with a rated input current up to and together with sixteen A per section which are meant to be related to the public mains community.

besides altering the energy filter to accommodate the frequency range increase, it may well be integral for manufacturers to redesign the vigour supply circuit with a purpose to no longer affect the sine wave exceptional of the public mains community or the product harmonics on the public mains community.

Voltage Fluctuations and Flicker. IEC 61000-3-three, obstacles of voltage fluctuations and flicker, is the different new emissions requirement. It specifies the trying out and boundaries of short interruptions or dips in the supply voltage caused by using other equipment related to the equal electrical supply (called flicker). the new requirement specifies that compliance have to be determined for all clinical electrical device or methods with a rated enter current up to and including sixteen A per phase and those that are intended to be related to the public mains community.

If the machine has lengthy-time and short-term existing ratings, the better of both ratings will be used in picking theapplicability of the requirement.

manufacturers may still observe that the holdup instances for vigour supplies will should be enhanced in machines for which voltage dips and interruptions may cause the product to lose characteristic.

conducted RF Immunity. There are several new immunity necessities within the new IEC document. the first is a brand new average for measuring carried out disturbances prompted by RF fields in delivery frequency: IEC 61000-4-6. under this regular, machine is evaluated in response to its respective testing class; these categories consist of life-helping device, non-lifestyles-helping gadget, shielded-vicinity-use equipment, intentional RF receivers, and battery-powered machine. producers are accountable for picking out the acceptable examine and severity stage relevant to the product.

Magnetic box Immunity. using IEC 61000-4-eight to check magnetic-field immunity at a considerable number of power frequencies is a different new immunity requirement below IEC 60601-1-2. equipment rated for both 50 and 60 Hz is subjected to a magnetic box of three A/m at 50 Hz and once more at 60 Hz. If a piece of machine is rated for operation at only one frequency, the assessments are performed on the rated frequency. There is not any allowance for lack of efficiency or interruption of operation in this requirement.

The manufacturers most effected with the aid of this new examine requirement can be these with gadget containing magnetic-sensing devices, equivalent to corridor-effect sensors or bimetal switches. certain defensive of those add-ons can be required to reduce unwanted operation. Magnetic container immunity stages can also also deserve to be raised for equipment intended to be used in the proximity of powerful magnetic fields.

Voltage Dips, Interruptions, and adaptations. a third new immunity requirement outlined in IEC 61000-4-eleven defines immunity test methods and the latitude of favored verify degrees for voltage dips, brief interruptions, and voltage adaptations of gadget connected to low-voltage energy provide networks. The requirement applies to equipment and systems which have an enter power ranking of as much as 1 kVA, or an input current of 16 A or much less per phase. There isn't any allowance for component screw ups or device malfunctions requiring repairs.

There is some leeway in the compliance ranges for non-life-aiding equipment, if the manufacturer can justify lessen ranges according to the hazard the product will pose when uncovered to voltage dips or short interruptions within the supply voltage. If a reduce compliance stage is sought and justified by using the company, it may well be essential to make use of (or make options for the use of) uninterruptible energy supplies, batteries, or power-conditioning device.

critical next steps

producers should act now to ensure their readiness for the brand new requirements in 60601-1-2. the following information are measures that groups can take to aid put together themselves.

examine products presently beneath development. manufacturers may still begin to determine knowledge noncompliance in products that are below building by way of checking out them against the latest IEC typical in a ten-m semianechoic chamber. probably right-funds-incomes items should still be identified and demonstrated immediately to examine what adjustments—if any—can be essential before the new version of the normal is formally established.

accomplice with a third-birthday party trying out lab as soon as feasible. checking out of medical instruments or methods requires time to complete the conformity evaluation section. most effective a number of conformity evaluation businesses permitted to function the checking out exist to serve a whole bunch of manufacturers. What's more, few labs are fitted with the entire array of test equipment obligatory to determine compliance with the new regular. To stay away from production delays, producers may still work with a 3rd-celebration tester to be sure that their most vital items are both compliant—or very shut—by means of November 1, 2004.

improve tables of applicable standards for each and every working mode. The tables should identfy viable indications of performance degradation and describe how such degradation is probably going to manifest itself. This assistance will aid the testing lab in detecting problems objectively so they can be accurately suggested to the brand. it will even be sensible for the company to witness the immunity exams so that noncritical blunders are correctly interpreted as such. producers seeking assistance in finishing these tables will improvement from an early partnership with their third-celebration look at various lab.

decide whether or now not to continue providing legacy items. producers should make selections quickly about legacy items, for which redesigning for compliance may be charge-prohibitive. Older products could should be replaced with redeveloped models to meet the brand new average.

investigate CE Marking. Following a a success product conformity reassessment, the statement of conformity for those gadgets previously bearing the CE marking will should be renewed and the technical files will should be revised, along with the device master information and design heritage files. The vital notified body (for devices in category I, IIa, IIb, or III) will should be counseled of any big design changes, and it may well be essential to resubmit a abstract of alterations made, along with a possibility evaluation and elementary requirements guidelines.

by means of maintaining abreast of the changes within the new EN EMC regular and Getting ready products for compliance, manufacturers can keep away from important time-to-market delays and benefit a world competitive part.

Don Sherratt is the director of company and technology for medical contraptions at Intertek ETL SEMKO in Boxborough, MA.

Copyright ©2002 scientific machine & Diagnostic business


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