CAN CSA-C22 2 NO 601 2 10-1992 Medical Electrical Equipment Part 2 Particular Requirements for the Safety of Nerve and Muscle Stimulators (First Edition General Instructions No 1-2.pdf

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1、CAN/CSA-C22.2 No. 601.2.10-92 (lEG 601-2-10:1987) (Reaffinned 1997) Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators A National Standard of Canada sJa.ijn)pJod uiosaq sa uapuo awiou osia5nfapinos.:,qn,j , eqwoui/nb4uaai ap uoiodwj uopzxjjddo

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24、suoun siapeai siawnsuoD siainpejnuew u!pnpu! s.iasn pue sianpo.id o snsuasuo ieuou e pajai spiepues j saqA!pc uoepi.iaD pu 2uawdoaAap sp.ipus ui pa6e6ua uojeposs d!qsiaqwaw XJeWnoA (iortieisuou i.joid-ioj-ou s L61 ui was spiepue iuoi aip o epwrj o punoj spiepue aip i(q papa.zxe pu 6L61 u paai.ap 5CM

25、 panpoid uaaq seLl p.epues uoIeN n saidsnc asoqapun (wa) iuocwwawi awu ipiapun swdo ipppvi uopcposs spapues uweu aqj. General Instruction No. 2 CAN/CSA-C22.2 No. 601.2.10-92 October 1992 CSA Standard CAN/CSA-C22.2 No. 601 .2.1 0-92, Medical Electrical Equipment Part 2: Particular Requirements for th

26、e Safety of Nerve and Muscle Stimulators, was published in August 1992: it consisted of 32 pages (15 preliminary and 1 7 text). Errata to the Editorial Changes to Appendix AA and to the Technical Deviation to Subclause 6.8.2 have been incorporated (and identified by a vertical line in the margin) in

27、 the attached replacement pages. CSA Standard CAN/CSA-C22.2 No. 601.2.10-92 now consists of the following pages: lx, xlii, xiv and 117 dated August 1992; and xi, xii and xv dated October 1992. These replacement pages are to be inserted into your copy of the Standard; the pages replaced should be kep

28、t for reference. Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Neive and Muscle Stimulators CAN/CSA-C22.2 No. 601.2.10-92 Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators Canadian Deviations and Editorial Cha

29、nges Notes: (1) Deviations in the technical requirements of the Particular Standard, initiated by the CSA committee, are indicated by Technical Deviation. (2) Editorial changes in text of the Particular Standard, initiated by the CSA committee, are indicated by Editorial Change. Sub-clause 1.1 Scope

30、 Technical Deviation Replace the existing first paragraph of this Sub-clause with the following text: This Particular Standard specifies requirements for the safety of NERVE AND MUSCLE STIMULATORS as defined in Sub-clause 2.1 .101, hereinafter referred to as EQUIPMENT, having a RATED OUTPUT POWER no

31、t exceeding 500 W and designed to be installed and used in accordance with the Rules of the Canadian Electrical Code, Part!. Editorial Change Add the following text to this Sub-clause: The requirements of this Particular Standard are in addition to those of CSA Standard CAN/CSA-C22.2 No. 601.1, Medi

32、cal Electrical Equipment Part 1: General Requirements for Safety, hereinafter referred to as the General Standard. For the purposes of testing and approving EQUIPMENT covered within the scope of this Particular Standard, the EQUIPMENT must meet the combined requirements, as applicable, of both this

33、Particular Standard and the General Standard. Editorial Change In this Particular Standard, “shall“ indicates a mandatory requirement; “should“ indicates a recommendation, or that which is advised but not mandatory. Editorial Change This ParticularStandard covers only nerve and muscle stimulators us

34、ed for the diagnosis and/or therapy of neuromuscular disorders. Sub-clause 4.1 Type tests and routine tests Editorial Change Due to the publication of the second edition of the Genera! Standard (CAN/CSA-C22.2 No. 601.1), this Sub-clause within the Particular Standard is no longer operative. No longe

35、r applicable, Appendix B has been deleted from the General Standard. I October 1992 XI (Replaces p. xi, August 1992) CAN/CSA-C22.2 No. 601.2.10-92 Sub-clause 5.1 Classification Editorial Change Due to the publication of the second edition of the General Standard (CAN/CSA-C22.2 No. 601.1), this Sub-c

36、lause within the Particular Standard is no longer operative. Delete the IEC Amendment. Class Ill equipment has been deleted from the General Standard. Sub-clause 6.8.2 Instructions for use Technical Deviation Additional Item. aa) The instructions for use shall additionally contain: g. Advice on the

37、preparation of the PATIENT, including skin preparation, and the use of conductive gel (if applicable) to provide effective patient contact. h. Advice on precautions and contraindications, including transthoracic stimulation. Sub-clause 6.8.3 Technical description Technical Deviation Additional Item.

38、 bb) The technical description shall additionally give: a. The polarity of the output (where applicable). b. The maximum output charge per pulse and maximum average current across a 500 ohm resistive load and at the maximum output setting. c. A graphical representation of typical output signals, sho

39、wing voltage and current waveforms, at half and full settings of the output control when the EQUIPMENT is operating in an open-circuit load condition and the EQUIPMENT is connected to resistive loads of 200 ohms, 500 ohms, 1000 ohms and 2000 ohms. Sub-clause 7.3 Power input Editorial Change The publ

40、ication of the second edition of the General Standard (CAN/CSA.C22.2 No. 601.1) has necessitated the following change to this Sub-clause in the Particular Standard. The Amendment to Sub-clause 7.3 should refer to Sub-clause 7.1 Item a). Sub-clause 7.3 is no longer used in the General Standard. Sub-c

41、lause 14.3 Editorial Change Due to the publication of the second edition of the General Standard (CAN/CSA-C22.2 No. 601.1), this Sub-clause within the Particular Standard is no longer operative. This Sub-clause is no longer used. Class Ill equipment has been deleted from the General Standard. xii Oc

42、tober 1992 (Replaces p. xii, August 1992) Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Neive and Muscle Stimulators Section Nine Fault Conditions Causing Overheating and/or Mechanical Damage; Environmental Tests Editorial Change The publication of the second edition

43、 of the General Standard (C4N/CSA-C22.2 No. 601.1) has necessitated the following change to this Section in the Particular Standard. The title has been changed to “Abnormal Operation and Fault Conditions; Environmental Tests“ in the General Standard. Sub-clause 57.3 Mains supply cables or cords Edit

44、orial Change The publication of the second edition of the General Standard (CAN/CSA-C22.2 No. 601.1) has necessitated the following change to this Sub-clause in the Particular Standard. The title has been changed to “Power supply cords“ in the General Standard. Appendices Editorial Change The public

45、ation of the second edition of the General Standard (CAN/CSA-C22.2 No. 601.1) has necessitated the following change to these Appendices in the Particular Standard. Appendix B is no longer used. Appendices C, D, E, F, and G of the General Standard apply. Appendices H and I are no longer used. Appendi

46、x AA Rationale Sub-clause AA5.1 Editorial Change The publication of the second edition of the General Standard (CAN/CSA-C22.2 No. 601.1) has necessitated the following change to this Sub-clause in the Particular Standard. Delete the first sentence. Sub-clause AA14.3 Editorial Change The publication

47、of the second edition of the General Standard (CAN/CSA-C22.2 No. 601.1) has necessitated the following change to this Sub-clause in the Particular Standard. Delete the sentence. October 1992 XV (Replaces p. xv, August 1992) General Instruction No. 1 CAN/CSA-C22.2 No. 601.2.10-92 August 1992 CSA Stan

48、dard CAN/CSA-C22.2 No. 601 .2.1 0-92, Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators, consists of 32 pages (1 5 preliminary and 1 7 text). This Standard, like all CSA Standards, is subject to periodic review, and amendments in the form of

49、replacement pages may be issued from time to time; such pages will be mailed automatically to those purchasers who complete and return the attached card.* Some Standards require frequent revision between editions, whereas others require none at all. It is planned to issue new editions of the Standard, regardless of the amount of revision, at intervals not greater than 5 years. Except in unusual circumstances, replacement pages will not be issued during the last year

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