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EMC DES-1D11 : Specialist, Technology Architect | Midrange Storage Solutions Exam

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Test Number : DES-1D11
Test Name : Specialist, Technology Architect | Midrange Storage Solutions
Vendor Name : EMC
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DES-1D11 exam Format | DES-1D11 Course Contents | DES-1D11 Course Outline | DES-1D11 exam Syllabus | DES-1D11 exam Objectives

Exam Name Dell EMC Certified Specialist - Technology Architect - Midrange Storage (DECS-TA)
Exam Code DES-1D11
Duration 120 mins
Number of Questions 60
Passing Score 60%
Official Training Dell EMC Midrange Storage Solutions Learning Center (MR-7TN-MSSLC)

Dell EMC Midrange Architectures - Identify and describe the Unity hardware (e.g., enclosures, I/O components, storage media options, etc.)
- Explain Unity storage resources and features (e.g., dynamic pools, RAID functions)
- Identify and describe SC Series storage resources, connectivity options (e.g., RAID, Consistency Groups, SSD, HDD options), and use cases
- Identify and describe the various controller options available in the SC Series models 25%

Dell EMC Midrange Product Solutions - Identify key features of the SC Series operating system
- Describe SC Series cross-platform replication functionality and use cases
- Describe how to provision and access Unity storage; including Block, Files, and VMware datastores
- Identify Unity advanced features for Block storage; e.g, FAST Suite, D@RE, host I/O limit availability, thin clones
- Identify Unity advanced features for File storage; e.g, IP Multi-tenancy, Advanced Static Routing, IP Packet Reflect, etc.
- Identify and describe Unity Data Protection (e.g., Snapshots, Replication, and Snapshot Replication architecture) solutions and use cases
- Describe Unity Data Mobility features, requirements, and use cases

- Compare and contrast similar features between the Unity and SC Series products 42%
Dell EMC Midrange Best Practices, Sizing, and Design - Apply Dell EMC midrange best practice recommendations for data service, system, storage, and host application configurations
- Identify and describe the sizing and design considerations for Unity and SC Series features
- Identify and describe how to size and design a midrange solution for performance, capacity, security, and resilience
- Describe the data gathering methods to size and design an SC Series solution
- Identify and describe the tools and resources available to size and design Unity and SC Series solutions
- Explain how to size an SC Series solution that includes Tiers 1-3, storage requirements, front-end and back-end connections, and common use cases

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EMC exam Questions

innovations for Bench testing medical gadgets | DES-1D11 PDF Dumps and Test Prep

originally published MDDI April 2003

trying out

For successful checking out, choose the right assessments and habits them on the appropriate time—in an appropriate facility.

by Robert Mosenkis

medical instruments can be Tested at a number of tiers in their life cycle. all through their preliminary design, it is essential for the design team to verify at least some facets of efficiency or safety to be sure that they're on the appropriate track. greater-extensive prototype testing usually follows completion of the preliminary design phase, to display that the machine meets its design standards. scientific trials may also observe.

trying out for regulatory approval, to fulfill the pointed out or implicit necessities of one or more regulatory organizations, is performed next; this may still be accomplished on production units or on preproduction prototypes that reflect the manufactured product. once a device has earned approval, production line birth-up frequently requires further trying out to validate the production equipment (as an example, samples from each and every cavity of a mildew) and inspection protocols. 

Later in the lifestyles cycle, the advertising department could request product-trying out facts to be used in brochures or on the company net website. Comparative trying out is occasionally acceptable; independent single-product trying out may also suffice. additionally, if design or material changes are ever made to the machine that might have an effect on efficiency or defense, further trying out is warranted, even if a new regulatory submission isn't required.

finally, additional testing may observe a mentioned adverse incident, to check what went wrong and why. many of the special considerations associated with this selected circular of checking out are past the scope of this article; however, the information introduced right here can also still show advantageous.

every circular of checking out requires a different method. Failure to Boost the foremost strategy for every might influence in even more trying out at a later time, or failure of the test consequences to meet the normal goal. as an instance, the usage of an latest commonplace to test a different equipment characteristic or technology may well be inappropriate. 

An instance of this happened when a company become asked to evaluate the resistance of several surgical masks to blood penetration. on the time, the only existing necessities have been for water-repellent fabric below prolonged exposure or materials subjected to liquid under force—these were not proper. To clear up the difficulty, the business developed an easy verify methodology that worried squirting animal blood from a syringe for a short while.

All stakeholders should ask three primary questions when establishing a checking out strategy:

• What tests are necessary?• What gadgets may still be confirmed, and when?• Who should still do the trying out?

a superior method will emerge as these questions are discussed and answered.

What exams Are essential?

The purpose of the trying out determines what checks are needed. whether it is early within the design cycle, using crude look at various setups just to examine that the machine will operate its fundamental function will doubtless suffice. For an electrocardiographic (ECG) computer screen, for example, attaching electrodes to a volunteer (or the design engineer) and displaying the output on an oscilloscope can reveal whether the waveform looks like a typical ECG; comparing the cost reveal in opposition t palpated pulse will display no matter if the fee meter is functioning. Electromagnetic compatibility (EMC) testing, as an example, is obviously now not warranted at this stage. Later, the design can also be established towards the complete necessities of a critical usual or against every of the product standards.

The question of even if to test towards recognized requirements or to advance a special check methodology depends upon who will evaluation the results. specifications are written to yield consistent consequences, no rely who applies the usual, or when. here's why so many requirements require complicated, exact, and often expensive test setups, as is the case with a currently developed usual for the blood-resistance checking out of surgical masks mentioned previous. while cautious testing to requirements is “overkill” within the initial design testing, it's often the most beneficial strategy in a while.

In some circumstances, the most suitable strategy is to alter a common. for instance, an ISO ordinary includes checks for leaks in luer fittings under power or vacuum. The fitting is attached to a delegated stainless-steel becoming, and drive or vacuum is utilized. however some safety syringes can also be used simplest with their manufacturers' proprietary needles and don't encompass luer fittings. since the concept of a leak-free connection would practice to these gadgets as well, it's appropriate to adjust the typical via substituting the proprietary needle and its fitting for the ordinary metal fitting and applying the force and vacuum specific within the standard.

in case your device makes use of a new know-how or comprises a novel characteristic, you may have no option but to increase a new check formulation, for the reason that standards conveniently do not follow. yet another instance for which trying out to a typical may no longer be the foremost method is when items are being in comparison for advertising purposes. because the outcomes are intended for the consumer, it may well be more desirable to simulate scientific use, rather than to make use of examine machine or fixtures which are average of these mandated by standards. 

custom check methods may look crude when in comparison with the distinctly advanced methodology of standards. besides the fact that children the previous may lack repeatability, and the techniques of diverse examine personnel can have an effect on the results, such shortcomings are not an element when all testing is achieved at one time and area, by the identical people.

What devices should still Be validated, and When?

The checking out intention will commonly dictate which, and the way many, contraptions to check, as well as when within the existence cycle to do the checking out. Prototypes are often built the usage of materials and recommendations quite distinct from these utilized in creation; they're constantly handcrafted and finely tuned. one of the tests which are significant to production devices aren't relevant at this stage; however, be aware of the lure hidden of their postponement.

Some assessments that are required for a finished product contain aspects of the machine that aren't worried in general use. EMC comes to mind, as do intense storage and working circumstances and biocompatibility. while it's handy to extend these assessments except the design is frozen, the can charge of alterations dictated by examine screw ups at that element can be high. In some such cases, the solution may be a further round of checking out, with the conception that one of the a success test outcomes should be would becould very well be valid later, particularly if design alterations don't seem to be necessary.

where the intention of trying out is regulatory approval (see sidebar), the test samples need to replicate creation devices for the consequences to be valid. The goal of this checking out is to exhibit that a quality machine can be continually produced. therefore, these tests should be accomplished best after the design procedure is finished; youngsters, as mentioned past, it might not be integral to repeat some previous assessments. 

The variety of samples established may neatly be dictated through the usual or tenet used. Relevance and/or statistical significance are top concerns. checking out a single pattern of a posh electronic equipment is constantly satisfactory for regulatory approval; testing 20 samples of a mass-produced machine can be needed to reveal uniformity. When choosing samples, they may still be as varied as indispensable (for example, samples from every construction line or each mould cavity), but consistent with the checking out goal.

Who may still Do the checking out?

In most cases, someone popular with the device and its application may still test the product; this continually elements to doing so in-condo. In bigger firms, a separate group can conduct all checking out; in smaller ones, it can fall to the design engineer, at the least for initial checking out. Some agencies don't realize that self-testing might also even be carried out when the file is protected in a 510(ok)––however here's now not always the case for different regulatory companies. If trying out is accomplished in-house, it's a good suggestion to have the examine plan reviewed via a person who is not too near the design, lest anything be inadvertently neglected.

It is a part of some organizations' high-quality processes to have an outdoor laboratory function closing testing, to make sure objectivity. however when an outdoor lab is used, it'll be one with experience in checking out scientific devices that is aware the purpose of the trying out and the character of the machine being proven. A scientific equipment firm once submitted the simplest prototype of its digital equipment to a native check condominium for vibration and have an effect on testing. unfortunately, that lab's advantage become in trying out for aerospace applications, and the impact verify that it advised demolished the pattern.

The main reason for the usage of an out of doors test condo is that the test requires really expert equipment. Biocompatibility, tensile strength, environmental, and EMC trying out are examples for which the device and amenities are too costly for the occasional needs of most clinical machine enterprises. but even less demanding examine gadget—and the abilities to make use of it––could now not be essential commonly enough to justify purchase.

impartial check residences can present a couple of other benefits, together with the following:

• Familiarity with requirements, including abilities of normal interpretations or upcoming changes.• The objectivity to critique a corporation's verify protocols.• journey with regulatory company expectations of testing.• checking out event with similar gadgets, that could support in test setup and efficiency.• Credibility with gadget clients––particularly when comparative checking out is carried out for marketing applications.

Some companies are involved concerning the confidentiality of proprietary suggestions that's shared with a test residence, in particular one which has labored for its competitors. while most verify labs can be chuffed to signal nondisclosure agreements, bear in mind that a lab depends on its attractiveness of integrity to survive and a single lapse will smash this attractiveness. So or not it's probably the lab might be self-encouraged to maintain its consumers' confidentiality. also, the very proven fact that a lab has validated a similar equipment for a competitor makes it more desirable capable of serve you.


As is right of numerous other endeavors, cautious planning is likely one of the most critical elements of a clinical gadget testing task. selecting the acceptable tests and conducting them on the proper times, in an acceptable facility, can enhance the product building and advertising and marketing system. 

Copyright ©2003 clinical machine & Diagnostic Industrya

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