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IEC 60601-2-10*CEI 60601-2-10

Medical electrical equipment; part 2: particular requirements for the safety of nerve and muscle stimulators

Số trang: 35
Ngày phát hành: 1987-00-00

Liên hệ
In addition to the requirements already contained in the General Standard this particular one contains only special safety requirements. Not applicable to equipment which is intended to be implanted or to be connected to implanted electrodes, intended for the stimulation of the brain, for neurological research, cardiac pacemakers, use during surgical procedures, averaged evoked potential diagnosis, electromyography, cardiac defibrillation, only for a transcutaneous nerve and muscle stimulator for pain relief and for body-worn equipment. Appendix B contains a procedure for testing during the manufacture and/or installation and appendix AA the rationale.
Số hiệu tiêu chuẩn
IEC 60601-2-10*CEI 60601-2-10
Tên tiêu chuẩn
Medical electrical equipment; part 2: particular requirements for the safety of nerve and muscle stimulators
Ngày phát hành
1987-00-00
Trạng thái
Hết hiệu lực
Tiêu chuẩn tương đương
DIN EN 60601-2-10 (2003-04), IDT * DIN VDE 0750-219 (1989-07), IDT * ABNT NBR IEC 60601-2-10 (1997-10-30), IDT * BS EN 60601-2-10 (1988-10-31), IDT * EN 60601-2-10 (2000-11), IDT * prEN 60601-2-10 (1999-08), IDT * NF C74-313 (2001-11-01), IDT * HD 395.2.10 S1 (1989-01), IDT * JIS T 0601-2-10 (2005-03-25), MOD * CAN/CSA-C22.2 No. 601.2.10-92 (1992-08-31), NEQ * SEV-ASE 1084-2-10 (1989), IDT * SN EN 60601-2-10 (2000-11), IDT * OEVE HD 395.2.10 S1 (1990-10-16), IDT * OEVE/OENORM EN 60601-2-10+A1 (2003-12-01), IDT * PN-EN 60601-2-10 (2002-08-15), IDT * PN-EN 60601-2-10 (2006-10-06), IDT * SS-IEC 601-2-10 (1988-09-14), IDT * SS-EN 60601-2-10 (2001-03-30), IDT * UNE 20613-2-10 (1992-12-02), IDT * UNE-EN 60601-2-10 (2001-09-21), IDT * GOST R 50267.10 (1993), IDT * GOST 30324.10 (1995), IDT * TS EN 60601-2-10 (2004-04-29), IDT * CEI 62-24 (1988), IDT * STN EN 60601-2-10 (2001-08-01), IDT * STN EN 60601-2-10 (2002-07-01), IDT * CSN EN 60601-2-10 (2001-08-01), IDT * JS 60601-2-10 (2012-08-01), IDT * NEN-EN-IEC 60601-2-10:2000 en;fr (2000-12-01), IDT * SANS 60601-2-10:2011 (2011-02-28), IDT
Tiêu chuẩn liên quan
Thay thế cho
Thay thế bằng
IEC 60601-2-10*CEI 60601-2-10 (2012-06)
Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators
Số hiệu tiêu chuẩn IEC 60601-2-10*CEI 60601-2-10
Ngày phát hành 2012-06-00
Mục phân loại 11.040.60. Thiết bị chữa bệnh
Trạng thái Có hiệu lực
Lịch sử ban hành
IEC 60601-2-10*CEI 60601-2-10 (2012-06)
Medical electrical equipment - Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulators
Số hiệu tiêu chuẩn IEC 60601-2-10*CEI 60601-2-10
Ngày phát hành 2012-06-00
Mục phân loại 11.040.60. Thiết bị chữa bệnh
Trạng thái Có hiệu lực
* IEC 60601-2-10*CEI 60601-2-10 (1987)
Medical electrical equipment; part 2: particular requirements for the safety of nerve and muscle stimulators
Số hiệu tiêu chuẩn IEC 60601-2-10*CEI 60601-2-10
Ngày phát hành 1987-00-00
Mục phân loại 11.040.60. Thiết bị chữa bệnh
Trạng thái Có hiệu lực
Từ khóa
Definitions * Dielectric strength * Electric appliances * Electrical engineering * Electrical medical equipment * Electrical safety * Electromagnetic compatibility * Electromedicine * Electrotherapy equipment * EMC * Equipment safety * Human medicine * Inscription * Inspection * Instructions for use * Interference rejections * Marking * Medical equipment * Medical sciences * Muscles * Nerves * Output-value * Protection against electric shocks * Rated current * Safety * Safety engineering * Safety requirements * Specification (approval) * Stimulators * Temperature * Testing * Voltage fluctuations
Mục phân loại
11.040.60. Thiết bị chữa bệnh
Số trang
35

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