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EMC DES-1721 : Specialist - Implementation Engineer, SC Series Exam

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Test Number : DES-1721
Test Name : Specialist - Implementation Engineer, SC Series
Vendor Name : EMC
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DES-1721 exam Format | DES-1721 Course Contents | DES-1721 Course Outline | DES-1721 exam Syllabus | DES-1721 exam Objectives


Exam Title : Dell EMC Certified Specialist - Implementation Engineer - SC Series
Exam ID : DES-1721
Exam Duration : 90 mins
Questions in exam : 60
Passing Score : 63%
Official Training : Dell EMC SC Series Implementation and Administration (ES102STG00702)
Exam Center : Pearson VUE
Real Questions : Dell EMC SC Series Specialist Implementation Engineer Real Questions
VCE practice exam : Dell EMC DES-1721 Certification VCE Practice Test

Storage Center Fundamentals
- Identify and describe the Dell Storage Center core features, licensed features, and user interfaces 5%
Storage Center Hardware
- Identify and describe the characteristics of the SC Series Controllers
- Identify and describe the characteristics of the SC Series disk enclosures 15%
Storage Center Cabling
- Describe front-end cabling best practices for Fibre Channel and iSCSI protocols and explain the types of redundancy for front-end cabling
- Describe how to create fault domains and their purpose
- Identify and describe virtual port zoning best practices
- Describe the SAS back-end cabling best practices 19%
Storage Center Deployment and Initial Configuration
- Describe how to prepare the installation environment and perform the initial setup and post-setup tasks on the Storage Center array 3%
Initial SAN HBA and Switch Configurations
- Identify and describe how to establish a connection between the host and SC Series Storage array through FC and iSCSI SAN
- Describe the best practices and characteristics for specific FC switch vendors, such as Brocade, when connecting to an SC Series Storage array 11%
Storage Center Basic Administration
- Describe how to create and use volumes and volume folders and how to perform management operations such as copy, mirror, migrate and expand volumes on an SC Series Storage array
- Describe how to create and manage server objects and server folders, how to discover initiatiors, and how to map them to server objects on an SC Series Storage array
- Identify and describe how to map a volume to a server object, how to establish multipath conectivity, the recommended MPIO settings, and the steps to make a mapped volume available at the operating system level including VMware vSpere, Linux, and Microsoft
- Identify and describe the procedure(s) to failover and rebalance the SC Series Controllers 15%
Dell Storage Manager (DSM) Installation and Configuration
- Identify and describe how to install the Dell Storage Manager (DSM) software and how to use the DSM views
- Describe how to manage users and permissions in Dell Storage Manager (DSM) and describe user management best practices 9%
Dell Storage Manager (DSM) Administration
- Describe how to configure datapage size, SNMP and SMTP parameters, and upgrade the SC Series software and licenses
- Describe the Dell Storage Manager (DSM) monitoring and metering capabilities, how to review alerts, run reports and replace a failed disk 6%
Storage Center Data Progression, Data Instant Replay, and Remote Instant
Replay Management
- Explain how to enable, create, and use storage profiles
- Identify and describe the Data Progression functions and how to configure Data Progression using storage profiles
- Describe the functions of Replay Manager, a Data Instant Replay snapshot, and how to configure and manage Data Instant Replays
- Explain how to configure a Remote Instant Replay replication, how to create and activate a disaster recovery site, and how to restore the source on an alternate site
- Describe how to configure Live Volume 17%
This certification validates the ability to perform basic to intermediate skill level tasks in deploying and manage the Dell EMC SC Series storage products. This exam is a qualifying exam for the Specialist - Implementation Engineer, SC Series track. This exam focuses on the knowledge and activities involved in installing, initializing, configuring and testing the hardware and software of the Dell EMC SC Series Storage products.
Dell Technologies provides free practice questions to assess your knowledge in preparation for the exam. practice questions allow you to become familiar with the courses and question types you will find on the proctored exam. Your results on a practice exam offer one indication of how prepared you are for the proctored exam and can highlight courses on which you need to study and train further. A passing score on the practice exam does not ensure a passing score on the certification exam.

Storage Center Fundamentals (5%)
• Identify and describe the Dell Storage Center core features, licensed features, and user interfaces

Storage Center Hardware (15%)
• Identify and describe the characteristics of the SC Series Controllers
• Identify and describe the characteristics of the SC Series disk enclosures

Storage Center Cabling (19%)
• Describe front-end cabling best practices for Fibre Channel and iSCSI protocols and explain the types of redundancy for front-end cabling
• Describe how to create fault domains and their purpose
• Identify and describe virtual port zoning best practices
• Describe the SAS back-end cabling best practices

Storage Center Deployment and Initial Configuration (3%)
• Describe how to prepare the installation environment and perform the initial setup and post-setup tasks on the Storage Center array

Initial SAN HBA and Switch Configurations (11%)
• Identify and describe how to establish a connection between the host and SC Series Storage array through FC and iSCSI SAN
• Describe the best practices and characteristics for specific FC switch vendors, such as Brocade, when connecting to an SC Series Storage array

Storage Center Basic Administration (15%)
• Describe how to create and use volumes and volume folders and how to perform management operations such as copy, mirror, migrate and expand volumes on an SC Series Storage array
• Describe how to create and manage server objects and server folders, how to discover initiatiors, and how to map them to server objects on an SC Series Storage array
• Identify and describe how to map a volume to a server object, how to establish multipath conectivity, the recommended MPIO settings, and the steps to make a mapped volume available at the operating system level including VMware vSpere, Linux, and Microsoft
• Identify and describe the procedure(s) to failover and rebalance the SC Series Controllers

Dell Storage Manager (DSM) Installation and Configuration (9%)
• Identify and describe how to install the Dell Storage Manager (DSM) software and how to use the DSM views
• Describe how to manage users and permissions in Dell Storage Manager (DSM) and describe user management best practices

Dell Storage Manager (DSM) Administration (6%)
• Describe how to configure datapage size, SNMP and SMTP parameters, and upgrade the SC Series software and licenses
• Describe the Dell Storage Manager (DSM) monitoring and metering capabilities, how to review alerts, run reports and replace a failed disk Storage Center Data Progression, Data Instant Replay, and Remote Instant

Replay Management (17%)
• Explain how to enable, create, and use storage profiles
• Identify and describe the Data Progression functions and how to configure Data Progression using storage profiles
• Describe the functions of Replay Manager, a Data Instant Replay snapshot, and how to configure and manage Data Instant Replays
• Explain how to configure a Remote Instant Replay replication, how to create and activate a disaster recovery site, and how to restore the source on an alternate site
• Describe how to configure Live Volume



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EMC real questions

thoughts for Bench testing medical gadgets | DES-1721 PDF get and exam Braindumps

at the beginning published MDDI April 2003

checking out

For a hit testing, choose the appropriate checks and habits them on the right time—in an appropriate facility.

with the aid of Robert Mosenkis

medical gadgets can also be proven at quite a lot of tiers in their life cycle. all the way through their preliminary design, it's critical for the design team to examine as a minimum some facets of efficiency or safeguard to make sure that they are on the correct music. greater-extensive prototype trying out usually follows completion of the preliminary design section, to exhibit that the gadget meets its design requisites. scientific trials may additionally observe.

testing for regulatory approval, to meet the pointed out or implicit necessities of 1 or greater regulatory agencies, is carried out next; this may still be performed on production gadgets or on preproduction prototypes that mirror the manufactured product. as soon as a tool has earned approval, production line delivery-up commonly requires extra checking out to validate the production device (for instance, samples from each and every cavity of a mildew) and inspection protocols. 

Later in the lifestyles cycle, the advertising branch may request product-checking out statistics for use in brochures or on the business internet web page. Comparative testing is occasionally appropriate; impartial single-product checking out may additionally suffice. also, if design or material adjustments are ever made to the machine that could have an effect on performance or security, additional testing is warranted, even if a new regulatory submission isn't required.

ultimately, extra testing may follow a pronounced adverse incident, to verify what went wrong and why. many of the particular considerations linked to this certain round of trying out are past the scope of this article; besides the fact that children, the advice introduced right here can also nonetheless show useful.

every circular of checking out requires a unique approach. Failure to Boost the greatest strategy for each and every might outcomes in much more checking out at a later time, or failure of the examine results to meet the common goal. as an example, the use of an present commonplace to test a unique machine characteristic or expertise may well be inappropriate. 

An instance of this befell when a corporation changed into requested to examine the resistance of several surgical masks to blood penetration. on the time, the only present standards had been for water-repellent fabric beneath prolonged exposure or materials subjected to liquid below drive—these have been no longer relevant. To clear up the issue, the company developed a simple examine methodology that involved squirting animal blood from a syringe for a short while.

All stakeholders have to ask three primary questions when establishing a checking out method:

• What exams are mandatory?• What instruments may still be established, and when?• Who may still do the checking out?

a very good strategy will emerge as these questions are mentioned and answered.

What tests Are crucial?

The aim of the testing determines what exams are mandatory. whether it is early in the design cycle, the use of crude verify setups just to investigate that the machine will operate its fundamental function will seemingly suffice. For an electrocardiographic (ECG) computer screen, as an example, attaching electrodes to a volunteer (or the design engineer) and displaying the output on an oscilloscope can exhibit no matter if the waveform seems like a standard ECG; comparing the rate monitor in opposition t palpated pulse will display no matter if the cost meter is functioning. Electromagnetic compatibility (EMC) checking out, for example, is naturally now not warranted at this stage. Later, the design may also be established towards the whole requirements of a crucial standard or against every of the product standards.

The question of even if to test against recognized necessities or to increase a different look at various methodology is dependent upon who will overview the results. standards are written to yield consistent outcomes, no count who applies the ordinary, or when. this is why so many specifications require advanced, genuine, and sometimes expensive look at various setups, as is the case with a lately developed common for the blood-resistance checking out of surgical masks outlined prior. whereas cautious testing to standards is “overkill” within the preliminary design testing, it is frequently the superior approach afterward.

In some instances, the choicest approach is to adjust a common. as an instance, an ISO usual comprises checks for leaks in luer fittings beneath power or vacuum. The becoming is attached to a delegated stainless-steel becoming, and pressure or vacuum is applied. but some security syringes can be used best with their producers' proprietary needles and don't encompass luer fittings. since the concept of a leak-free connection would observe to those contraptions as well, it's applicable to alter the standard by using substituting the proprietary needle and its becoming for the ordinary metal fitting and applying the drive and vacuum specified in the standard.

in case your device uses a new know-how or comprises a novel function, you may additionally haven't any alternative however to strengthen a brand new check formula, in view that standards conveniently do not follow. one more instance for which checking out to a common may additionally no longer be the ultimate method is when items are being compared for advertising and marketing applications. because the effects are intended for the client, it may well be more suitable to simulate scientific use, rather than to use test equipment or fixtures that are standard of those mandated via requisites. 

customized verify methods may also appear crude when compared with the pretty advanced methodology of standards. although the former might also lack repeatability, and the thoughts of distinctive examine personnel can affect the outcomes, such shortcomings don't seem to be an element when all testing is completed at one time and location, through the equal americans.

What gadgets may still Be established, and When?

The checking out purpose will often dictate which, and how many, contraptions to examine, in addition to when within the existence cycle to do the trying out. Prototypes are sometimes constructed the usage of materials and innovations somewhat distinctive from those used in production; they are constantly handcrafted and finely tuned. probably the most assessments that are valuable to construction contraptions aren't applicable at this stage; despite the fact, be privy to the lure hidden in their postponement.

Some checks that are required for a comprehensive product involve facets of the equipment that are not involved in common use. EMC comes to mind, as do extreme storage and working conditions and biocompatibility. whereas it's handy to delay these checks until the design is frozen, the cost of adjustments dictated via examine failures at that point may be excessive. In some such instances, the answer should be would becould very well be an extra circular of testing, with the theory that probably the most a success test results could be valid later, above all if design changes don't seem to be obligatory.

the place the goal of testing is regulatory approval (see sidebar), the look at various samples need to mirror construction instruments for the effects to be valid. The goal of this trying out is to reveal that a quality device can also be normally produced. for this reason, these checks need to be finished best after the design procedure is complete; besides the fact that children, as mentioned past, it might now not be integral to repeat some outdated tests. 

The number of samples proven could well be dictated by means of the typical or guiding principle used. Relevance and/or statistical significance are major issues. checking out a single demo of a complex digital device is usually adequate for regulatory approval; checking out 20 samples of a heavily produced device may be needed to demonstrate uniformity. When selecting samples, they may still be as dissimilar as quintessential (as an example, samples from every creation line or each mold cavity), however in step with the checking out intention.

Who should Do the trying out?

In most cases, a person time-honored with the device and its software should still verify the product; this constantly facets to doing so in-apartment. In larger firms, a separate group can conduct all testing; in smaller ones, it may fall to the design engineer, at the least for initial checking out. Some organizations do not realize that self-testing might also also be executed when the file is protected in a 510(k)––although this is now not always the case for different regulatory corporations. If checking out is finished in-apartment, or not it's a good suggestion to have the test plan reviewed by means of someone who isn't too close to the design, lest whatever be inadvertently left out.

It is part of some businesses' first-class techniques to have an outside laboratory perform final trying out, to be sure objectivity. but when an outside lab is used, it'll be one with experience in trying out scientific contraptions that knows the purpose of the checking out and the nature of the gadget being established. A scientific equipment firm once submitted the only prototype of its electronic device to a local test condo for vibration and have an impact on checking out. unfortunately, that lab's abilities become in checking out for aerospace functions, and the impact verify that it recommended demolished the sample.

The leading explanation for the use of an outdoor verify condo is that the check requires specialized machine. Biocompatibility, tensile electricity, environmental, and EMC trying out are examples for which the machine and facilities are too expensive for the occasional wants of most medical gadget firms. but even less demanding check device—and the expertise to use it––might no longer be mandatory frequently ample to justify buy.

impartial verify houses can offer several other benefits, together with here:

• Familiarity with specifications, including potential of regular interpretations or upcoming alterations.• The objectivity to critique a company's examine protocols.• journey with regulatory company expectations of trying out.• testing adventure with similar instruments, that could support in verify setup and performance.• Credibility with machine users––especially when comparative checking out is accomplished for advertising purposes.

Some agencies are involved in regards to the confidentiality of proprietary counsel that's shared with a look at various condominium, especially one which has labored for its rivals. while most test labs may be chuffed to signal nondisclosure agreements, remember that a lab relies on its recognition of integrity to live on and a single lapse will damage this acceptance. So it be seemingly the lab could be self-influenced to maintain its customers' confidentiality. also, the very incontrovertible fact that a lab has established an analogous machine for a competitor makes it enhanced in a position to serve you.

Conclusion

As is right of countless other endeavors, cautious planning is without doubt one of the most important aspects of a clinical gadget checking out challenge. making a choice on the acceptable tests and conducting them at the relevant instances, in an appropriate facility, can boost the product development and advertising procedure. 

Copyright ©2003 clinical equipment & Diagnostic Industrya


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