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  1. TUV Questions
  2. 1. What is true statement of the EU guidelines
  3. a. Should allow free movement in EU of goods
  4. b. Only sold/operated in EU
  5. c. Manufacturer must issue
  6. d. Declaration of conformity
  7.  
  8. 2. What the CE mark is
  9. a. Quality – no
  10. b. Declaration of conformity – yes
  11. c. Optional – no
  12. d. Sold in the EU – yes
  13.  
  14. 3. Name required measures when a machine is modified
  15. a. Always attached a new CE mark – no
  16. b. Prepare documentation – yes
  17. c. Evaluate performance level of safety fn – no
  18. d. Inform the operating staff – yes
  19.  
  20. 4. Which statement true according to EU guideline
  21. a. Each country creates its own guidelines – no
  22. b. EU guidelines should guarantee free travel – yes
  23. c. They are recommendations – no
  24. d. Guidelines always refer to the application of standards – no
  25.  
  26. 5. When can a standard presume to conform to European guidelines
  27. a. When it is listed in the official journal of EU
  28.  
  29. 6. Name Hierarchy of standards
  30. a. Consequences of standards C->B->A
  31.  
  32. 7. Which are true
  33. a. Standards describe the current technology – yes
  34. b. ISO must be applied for CE marking – no
  35. c. Safety related standards are always listed in official journals of EU – no
  36. d. Standards are technical regulations with recommendations – yes
  37.  
  38. 8. Name corrective measures for foreseeable misuse
  39. a. Reconsideration of operating and safety concept – yes
  40. b. Involvement of safety experts when purchasing – yes
  41. c. Replacement of staff – no
  42. d. Installation of e-stop – no
  43.  
  44. 9. Which is true about risk assessment
  45. a. An EU declaration of conformity may not be issues in principle without a risk assessment – yes
  46. b. EN ISO 12100 always describes the identification of hazardous locations as adequate measures – no
  47. c. Machine must be designed and built under consideration of risk assessment – yes
  48. d. The purchaser of the machine receives the risk assessment document – no
  49.  
  50. 10. What is the highest PL that can be achieved with a individual relay or contactor
  51. a. C
  52.  
  53. 11. Is Category 2 a single channel structure
  54. a. No
  55.  
  56. 12. What are 3 ways to calculate MTTFd
  57. a. Manufacturers datasheets
  58. b. Calculate an estimate from Annex C
  59. c. Annex D
  60. d. Set to 10 years
  61.  
  62. 13. Is common cause failure applicable to Category 2
  63. a. Yes
  64.  
  65. 14. When is it necessary to use guards (separating protective device) on a machine
  66. a. When part are ejected – yes
  67. b. Radiation – yes
  68. c. At all access points to the machine – no
  69. d. When using lifting/rotary devices – no
  70.  
  71. 15. A moveable isolating device (guard locking switch) is configured so hazardous location can be reached before other risk has been minimized. What measures are suitable to reduce the residual risk
  72. a. Lock – yes
  73. b. Sign – no
  74. c. Interlocking device with guard locking – yes
  75. d. Light curtain – no
  76.  
  77. 16. Which is true with respect to OSSD
  78. a. OSSD signals of ESPE are maintained by ESPE itself – yes
  79. b. OSSD signals connected to safety PLC need no further diagnostics by safety PLC -no
  80. c. OSSD signals connected to safety PLC need to be monitored by cross checking – yes
  81. d. Using type-2 ESPE (performance level C) is sufficient to process 1 of the OSSD signals to reach performance level C – no
  82.  
  83. 17. How many positions does an enabling switch have – 3
  84.  
  85. 18. Which is true with respect to e-stop
  86. a. Disconnection of power is also permitted with electronic devices – yes
  87. b. The power is always disconnected in the event of an e-stop – no
  88. c. An e-stop can be implement by safe operating stop – no
  89. d. It is allowed to perform an estop in category 1 stop – yes
  90.  
  91. 19. What is true with respect to Category 3
  92. a. Accumulation of faults may not lead to loss of safety function – no
  93. b. Each fault must be detected before or at the next request of the safety function – yes
  94. c. The diagnostics for channel 1 may be carried out be other units than the logic unit of channel 2 – yes
  95. d. All faults must be detected – no
  96.  
  97. 20. Which is true
  98. a. If using module safety plc then it may be necessary to consider each modules individually in PL calc – yes
  99. b. Safety PLC need no consideration in PL calc – no
  100. c. It has to be ensured test function for sensors and actuators are activated in the logic – yes
  101. d. The deactivation of output test within safety PLC may have effects on test of other outputs – yes
  102.  
  103. 21. Which safety standard is responsible for drives
  104. a. EN 61800-5-2
  105.  
  106. 22. Which safety functions corresponds to stop categories EN 60204-1
  107. a. STO
  108. b. SS1
  109. c. SS2
  110.  
  111. 23. What are the appropriate measures to achieve the safety function STO
  112. a. Contactor between power supply and drive – yes
  113. b. Fuses in power supply phases of drive system – no
  114. c. Safe pulse inhibit – yes
  115. d. Setpoint selection via control PLC – no
  116.  
  117. 24. Which manufacturer data is required for safety function if you consider the drives as subsystem for determining the PL and there are no category requirements
  118. a. DC – no
  119. b. PFHd – yes
  120. c. CCF – no
  121. d. PL – yes
  122.  
  123. 25. Which standard defines the qualitative requirements for the complete lifecycle of safety related software
  124. a. IEC 1131 – no
  125. b. EN ISO 61800 – no
  126. c. EN ISO 13849-1 and 13849-2 - yes
  127. d. EN ISO 12100-1 – no
  128.  
  129. 26. What maximum performance level can be achieved using the safety related embedded software (SRESW) in accordance with EN ISO 13849-1
  130. a. PLb - no
  131. b. PLc - no
  132. c. PLd - yes
  133. d. PLe – no
  134.  
  135. 27. How can software faults be avoided
  136. a. Training – yes
  137. b. Redundant hardware – no
  138. c. Time management – yes
  139. d. Certified functional modules -yes
  140.  
  141. 28. The validation plan must contain the following
  142. a. Tools which are used for validation (test equipment) – yes
  143. b. All technical documents - no
  144. c. Operating conditions – yes
  145. d. List of safety functions – yes
  146.  
  147. 29. What forms part of the documentation of validation in accordance with 13849-2
  148. a. Manual of all components used in the machine – no
  149. b. Validation plan – yes
  150. c. Logs of the test records – yes
  151. d. Safety information for usage and possible limitations for the user – yes
  152.  
  153. 30. What must a validation show
  154. a. A validation must contain an analysis – yes
  155. b. A validation must show each SRP/CS subsystem meets the requirement of 13849-1 – yes
  156. c. The validation is limited to checking the safety function and the eschewed PL – no
  157. d. The validation must always be carried out through analysis and testing – no
  158.  
  159. 31. What must be noted about the response under fault conditions
  160. a. All the faults and failures are recorded in a list in EN ISO 13849-2 – no
  161. b. An FMEA (failure mode and effect analysis) must be carried out for faults and failures that are not listed in EN ISO 13849-2 – yes
  162. c. EN ISO 13849-1 defines common faults and failures – yes
  163. d. Further cases must be taken into account in addition to faults and failures according to 13849-2 – yes
  164.  
  165. 32. Which statements are correct
  166. a. The validation should be performed by the same person who is in charge of the design – no
  167. b. During the validation a check is made whether the system solution meets the user requirements – yes
  168. c. Using the IFA systema software covers all aspects of validation – no
  169. d. A component can be well tried for one application but unsuitable for another application – yes
  170.  
  171. 33. Give some examples of safety modules according to Annex V of the machinery directive MRL 2006/42/EC
  172. a. Pressure cut off valve against pressure intensification – no
  173. b. Logic unit to guarantee safety function -yes
  174. c. Ropes, chains, belts – no
  175. d. Pull-wire – yes
  176.  
  177. 34. Name the consequences of a thermal hazard (check the formulas)
  178. a. Frostbite – yes
  179. b. Bruising – no
  180. c. Dehydration – yes
  181. d. Mutation – no
  182.  
  183. 35. EN ISO 12100 describes the iterative process for risk reduction including risk assessment. Which measure must be carried out before the start of the process?
  184. a. Check: is there a C type standard for this machine? – yes
  185. b. No measure – no
  186. c. Check: is there a B type standard for this machine? – no
  187. d. Check: is there an A type standard for this machine – no
  188.  
  189. 36. Which of the name measures are proven safety principles
  190. a. Overdimensioning/safety factor – yes
  191. b. Positive mechanical action/operation – yes
  192. c. Use of de-energisation principle – no
  193. d. Protection against unexpected start-up – no
  194.  
  195. 37. Determination of the risk and the associated PLr. Which statements apply
  196. a. If in doubt, the higher value should be user for parameters S, F and P – yes
  197. b. The same PLr applies to all risks of a machine – no
  198. c. The risk graph of EN SIO 13849-1 only makes one possible option available for determining the PLr. Other options are also permitted. – yes
  199. d. The exact level of frequency of exposure to the hazard is required to determine the PLr. – no
  200.  
  201. 38. Which component can be used to implement a safety function
  202. a. Two-hand operator console - yes
  203. b. Contactor - yes
  204. c. Standard PLC – yes
  205. d. Laser scanner - yes
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