E22-214 - ScaleIO 1.x Server-Based SAN Exam Real Exam Questions and Answers
ScaleIO 1.x Server-Based SAN Exam
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Test Number : E22-214
Test Name : ScaleIO 1.x Server-Based SAN Exam
Vendor Name : EMC
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E22-214 test Format | E22-214 Course Contents | E22-214 Course Outline | E22-214 test Syllabus | E22-214 test Objectives
Exam Title :
Dell EMC Certified VxFlex OS 2.x Server-Based SAN (DEC)
Exam ID :
E22-214
Exam Duration :
90 mins
Questions in test :
60
Passing Score :
63%
Official Training :
VxFlex OS and Ready Node Implementation and Management (MR-1CP-SCLIOIM2)
Exam Center :
Pearson VUE
Real Questions :
Dell EMC VxFlex OS Server-Based SAN Real Questions
VCE practice questions :
Dell EMC E22-214 Certification VCE Practice Test
Dell EMC VxFlex OS Overview and Architecture 20%
- Describe the VxFlex OS architecture, components, and operation
- Explain the benefits and value proposition of a VxFlex OS solution
- Define how VxFlex OS solves data center problem use cases
Dell EMC VxFlex OS Installation 30%
- Describe how VxFlex OS is deployed in physical host environments
- Describe how VxFlex OS is deployed in VMware environments
- Identify how a VxFlex OS installation is deployed
Dell EMC VxFlex OS Configuration and Management 30%
- Describe how management interfaces for VxFlex OS are defined
- Explain how a VxFlex OS system is configured
- Describe how to create, map, and manage a volume
- Describe how system objects are defined
Dell EMC VxFlex OS Monitoring and Troubleshooting 20%
- Explain how a VxFlex OS cluster is monitored
- Describe how the basic troubleshooting for a VxFlex OS cluster is performed
- Describe how performance optimization for VxFlex OS is performed
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EMC outline
understanding the new EMC ordinary for scientific contraptions: What manufacturers should know Now | E22-214 test Braindumps and boot camp
at the beginning published MDDI August 2002
ELECTRONICS
knowing the new EMC normal for clinical devices: What manufacturers deserve to know Now
assembly the brand new requirements set forth in the latest edition of 60601-1-2 may show difficult for OEMs.
Don Sherratt
In 1993, the international Electrotechnical fee (IEC) posted the first version of 60601-1-2, the international electromagnetic compatibility (EMC) usual for scientific gadgets. quickly after, the ecu Committee for Standardization (CENELEC) adopted it as a eu Norm (EN) general—with simplest minor adjustments. it'll for this reason come as no shock that IEC's latest revision of 60601-1-2, posted in September 2001, turned into adopted through CENELEC almost immediately thereafter and posted as EN 60601-1-2:2001 it is going to seem within the legit Journal of the ecu community in August 2002.IEC (EN) 60601-1-2:2001 is regarded an immense rewrite of the customary and should have profound outcomes on compliance in regards to two critical eu directives: the lively Implantable clinical devices Directive (ninety/385/EEC) and the medical gadgets Directive (93/forty two/EEC), in addition to CB Scheme necessities and connected requirements. while the phaseout date of the 1993 EN typical may be two years from now, manufacturers that export their products globally—or who plan to—and want to continue to be aggressive may still automatically begin developing ideas to address the new standard's have an effect on on product design and development.
To aid producers put together for this transition, this text addresses essentially the most tremendous transformations between the first and 2d editions of IEC 60601-1-2, and outlines key steps to compliance.
more challenging criteria, larger limits
the most tremendous revisions to IEC 60601-1-2 include multiplied testing limits for electrostatic discharge (ESD), radiated radio-frequency (RF) immunity, surge immunity, and electrical quickly transients (EFTs). There are also required exams for carried out RF immunity, magnetic field immunity, voltage dips, harmonic distortion, and voltage flicker. moreover, the typical consists of greater-finished circulate/fail standards, which require that scientific utility be maintained throughout immunity checks and that the company outline proper standards of medical utility.
Electrostatic Discharge. The standard outlined in IEC 60601-1-2:2001 for measuring ESD is IEC 61000-four-2. It defines the range of look at various tiers in the case of diverse environmental and installing circumstances and establishes the acceptable look at various approaches. The aim of the average is to set up a common reproducible basis for evaluating the performance of gadget when subjected to ESD. table I compares the historical ESD dimension limits to the brand new ones.
IEC 60601-1-2:1993
IEC 60601-1-2:2001
IEC 801-2
IEC 61000-four-2
±3 kV for conductive materials±8 kV for nonconductive elements
±2, 4, and 6 kV for conductive materials±2, 4, and eight kV for nonconductive elements
desk I. A evaluation of ESD requirements between the old and new requirements.These new necessities will possible demand that insulation thicknesses and creepage and clearance distances be more suitable than earlier than to avoid arcing through and monitoring over insulation. They might additionally require enclosure materials to possess improved antistatic properties, or that equipment specifications special in person manuals mandate larger relative humidity tiers for working environments.
Radiated RF Immunity. within the first edition of the common, RF immunity necessities were defined by IEC 801-three. within the up to date edition, they're defined by means of IEC 61000-four-three and are outlined one after the other for life-aiding and non-lifestyles-aiding clinical electrical equipment. The frequency range of the requirements has been widened and permits for devices exact to be used handiest in shielded places. different noteworthy transformations include an intentional RF receivers' operation-mode exemption and a mandate that affected person-coupled machine ought to meet the identical requirements as different equipment. table II presents a assessment of the two standards.
There are distinctive verify methods defined within the new general for measuring RRFI of different clinical electrical device; manufacturers should talk about essentially the most suited methods with technical experts at their trying out lab.
IEC 60601-1-2:1993
IEC 60601-1-2:2001
IEC 801-3
IEC 61000-4-three
three V/m at ISM frequencies from 26 MHz to 1 GHz with eighty% AM for non-lifestyles-aid machinethree V/m from 26 MHz to 1 GHz with eighty% AM modulation for all times-support device
three V/m at ISM frequencies from eighty MHz to 2.5 GHz with 80% AM for non-lifestyles-help gadget10 V/m from eighty MHz to 2.5 GHz with 80% AM modulation for all times-help equipment
desk II. A evaluation of RF immunity necessities between the ancient and new necessities.Electrical quick Transients. IEC 801-four determined the EFT immunity requirements and check methods in the old ordinary, however will be replaced by way of IEC 61000-four-4 within the new version. the new usual defines the look at various voltage waveform, range of check levels, verify equipment, check setup, and examine method, as outlined in table III. One brilliant alternate is the inability of differentiation between completely and temporarily installed device. There also are gigantic modifications within the necessities for trying out degrees and repetition expense, and pass-fail criteria are plenty tighter below the brand new common.
manufacturers should still also be conscious that the brand new usual requires that handheld machine or components of handheld equipment be proven with a man-made hand to simulate the capacitive coupling impact of the operator, as specific in CISPR sixteen-1. The synthetic hand is linked to the ground reference airplane right through the assessments. This requirement is new for scientific electrical equipment and might effect in dielectric stresses on signal or patient cables carrying high-frequency or excessive-voltage signals. To in the reduction of the skills for this prevalence, producers should take into account the type of cables used in interconnecting leads and be aware that affected person leads could deserve to be changed.
IEC 60601-1-2:1993
IEC 60601-1-2:2001
IEC 801-4
IEC 61000-four-four
±1kV for mains-plug-classification machine±2kV for permanent device
±0.5 kV for sign lines
2.5-kHz repetition price
±2kV on vigor traces±1kV for sign traces
5-kHz repetition expense
desk III. A comparison of EFT requirements between the ancient and new requirements.Surge Immunity. IEC 61000-four-5 is the brand new general that specifies examine ranges relating to distinctive environmental and installing situations. It establishes a typical reference for evaluating the performance of equipment when subjected to excessive-energy disturbances on the energy and interconnection lines, and specifies sweeping phase angles over selected voltage ranges. The decision of compliance is in accordance with the response of the device, considering that every surge personally, and thinking of the effects of any coupling between cables which are Checked at once and those that don't seem to be. table IV items a assessment of the historical and the brand new requirements.
These new requirements may necessitate circuit redesign and component changes in scientific contraptions. whereas the upper voltage requirement remains the same, the brand new reduce voltage requirement skill a couple of degree of surge coverage will be essential and will should begin at ±0.5 kV.
New assessments, methods, and necessities
IEC 60601-1-2:1993
IEC 60601-1-2:2001
IEC 801-5
IEC 61000-four-5
±2kV normal mode±1kV differential mode
±1.5, 1, and a pair of kV average mode±0.5 and 1 kV differential mode
table IV. A comparison of surge immunity requirements between the old and new standards.moreover a significant difference in examine limits, the brand new general also specifies changes in the classification of items and outlines the strategies and new gadget indispensable to determine emissions and immunity compliance.
Product Classification. the new commonplace stipulates that nonmedical device used in a medical device want simplest meet the relevant CISPR requirements—in most circumstances CISPR 14, 15, and 22. Most medical electrical equipment or systems will stay discipline to the necessities of CISPR 11 and should be described as neighborhood 1 or 2 and sophistication A or B. manufacturers should still take into account that hospitals are sometimes considered residential or domestic; hence, class B limits are sometimes imposed.
Harmonic Distortion. There are two new requirements for choosing emissions compliance. the primary, IEC 61000-three-2, Limits for harmonic current emissions, addresses the effect on the sinusoidal waveform of the leading provide of products with a rated input existing up to and together with sixteen A per part that are intended to be related to the general public mains community.
besides changing the vigor filter to accommodate the frequency latitude raise, it could be vital for manufacturers to remodel the vigor supply circuit with the intention to not have an effect on the sine wave pleasant of the general public mains network or the product harmonics on the public mains network.
Voltage Fluctuations and Flicker. IEC 61000-3-3, boundaries of voltage fluctuations and flicker, is the different new emissions requirement. It specifies the testing and limits of brief interruptions or dips in the deliver voltage caused by different apparatus related to the identical electrical supply (called flicker). the new requirement specifies that compliance have to be determined for all medical electrical equipment or methods with a rated input latest as much as and including 16 A per phase and people that are intended to be connected to the general public mains community.
If the machine has lengthy-time and non permanent existing ratings, the larger of the two scores shall be used in selecting theapplicability of the requirement.
producers should still be aware that the holdup times for vigour elements will deserve to be stronger in machines for which voltage dips and interruptions can cause the product to lose function.
performed RF Immunity. There are several new immunity necessities within the new IEC doc. the first is a brand new commonplace for measuring conducted disturbances brought on with the aid of RF fields in delivery frequency: IEC 61000-4-6. below this regular, machine is evaluated according to its respective checking out class; these classes encompass lifestyles-aiding gadget, non-lifestyles-assisting machine, shielded-place-use gadget, intentional RF receivers, and battery-powered device. manufacturers are answerable for picking the acceptable examine and severity degree applicable to the product.
Magnetic field Immunity. the use of IEC 61000-4-8 to examine magnetic-container immunity at various power frequencies is a different new immunity requirement below IEC 60601-1-2. machine rated for both 50 and 60 Hz is subjected to a magnetic container of three A/m at 50 Hz and once again at 60 Hz. If a piece of equipment is rated for operation at only one frequency, the exams are carried out at the rated frequency. There is not any allowance for loss of performance or interruption of operation during this requirement.
The manufacturers most effected with the aid of this new check requirement might be those with device containing magnetic-sensing gadgets, equivalent to corridor-impact sensors or bimetal switches. selected defensive of these add-ons can be required to cut back undesirable operation. Magnetic field immunity degrees might also also deserve to be raised for machine supposed for use in the proximity of effective magnetic fields.
Voltage Dips, Interruptions, and diversifications. a 3rd new immunity requirement outlined in IEC 61000-4-11 defines immunity verify methods and the latitude of favourite verify stages for voltage dips, brief interruptions, and voltage adaptations of equipment related to low-voltage energy provide networks. The requirement applies to gadget and programs which have an input power score of up to 1 kVA, or an enter existing of sixteen A or less per section. There is not any allowance for element disasters or device malfunctions requiring repairs.
There is a few leeway within the compliance degrees for non-lifestyles-assisting machine, if the brand can justify lower stages in accordance with the hazard the product will pose when uncovered to voltage dips or brief interruptions within the provide voltage. If a lessen compliance stage is sought and justified with the aid of the brand, it may be imperative to use (or make strategies for using) uninterruptible power supplies, batteries, or energy-conditioning machine.
vital next steps
producers may still act now to be sure their readiness for the new necessities in 60601-1-2. here suggestions are measures that groups can take to aid put together themselves.
check items presently under building. producers may still start to determine knowledge noncompliance in items which are beneath construction via testing them in opposition t the existing IEC standard in a ten-m semianechoic chamber. doubtlessly true-cash-earning items should be recognized and established immediately to determine what changes—if any—will be critical earlier than the brand new edition of the regular is formally established.
companion with a 3rd-party checking out lab as quickly as possible. checking out of medical devices or systems requires time to complete the conformity evaluation se
