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YY 0951-2015 English PDF

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YY 0951-2015: Interferential current therapy instrument
Status: Obsolete

YY 0951: Historical versions

Standard IDUSDBUY PDFLead-DaysStandard Title (Description)Status
YY 0951-2015519 Add to Cart 3 days Interferential current therapy instrument Obsolete
YY/T 0951-2015289 Add to Cart 3 days Interferential current therapy instrument Valid

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YY 0778   YY/T 1095   YY 0950   YY/T 0323   YY/T 0952   

Basic data

Standard ID: YY 0951-2015 (YY0951-2015)
Description (Translated English): Interferential current therapy instrument
Sector / Industry: Medical Device & Pharmaceutical Industry Standard
Classification of Chinese Standard: C42
Classification of International Standard: 11.040.60
Word Count Estimation: 13,176
Date of Issue: 2015-03-02
Date of Implementation: 2017-01-01
Quoted Standard: GB/T 191-2008; GB 9706.1-2007; GB/T 14710-2009; GB/T 16886.1; YY/T 0466.1-2009; YY 0505; YY 0607-2007; YY 0868-2011
Adopted Standard: YY 0607-2007, MOD
Regulation (derived from): The State Food and Drug Administration Announcement 2015 No. 8
Issuing agency(ies): State Food and Drug Administration
Summary: This Standard specifies the interference therapy equipment terminology and definitions, classification, requirements, test methods, inspection rules, signs, instructions, packaging, transport and storage. 3.1 This Standard applies to equipment regulations.

YY 0951-2015: Interferential current therapy instrument

---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Interferential current therapy instrument ICS 11.040.60 C42 People's Republic of China pharmaceutical industry standards Interference therapy equipment Issued on. 2015-03-02 2017-01-01 implementation China Food and Drug Administration released

Foreword

This standard was drafted in accordance with GB/T 1.1-2009 given rules. The standard safety requirements for full implementation of the GB 9706.1-2007 "Medical Electrical Equipment Part 1. General requirements for safety," the content. This revised standard adopts YY 0607-2007 "Medical electrical equipment - Part 2. nerve and muscle stimulators for the safety requirements" Provisions. The standards for electromagnetic compatibility in accordance with the requirements of YY 0505 "Medical electrical equipment - Part 1-2. General requirements for safety - Collateral standard. EMC requirements and tests "to run concurrently. Please note that some of the content of this document may involve patents. Release mechanism of the present document does not assume responsibility for the identification of these patents. This standard was proposed by the China Food and Drug Administration. This standard by the National Technical Committee of Standardization for medical electrical physical therapy equipment at the Technical Committee (SAC/TC10/SC4) centralized. This standard was drafted. Tianjin, the State Food and Drug Administration Medical Device Quality Supervision and Inspection Center. The main drafters of this standard. Juan Yang, Han desert, Wu Chi-wai, Liu Bo, Li Yanan. Interference therapy equipment

1 Scope

This standard specifies the interference current therapy apparatus (hereinafter referred to as the device) terms and definitions, classification, requirements, test methods, inspection rules, marking Chi, instructions, packaging, transport and storage. 3.1 This standard applies to equipment regulations.

2 Normative references

The following documents for the application of this document is essential. For dated references, only the dated version suitable for use herein Member. For undated references, the latest edition (including any amendments) applies to this document. GB/T 191-2008 Packaging - Pictorial signs GB 9706.1-2007 Medical electrical equipment - Part 1. General requirements for safety GB/T 14710-2009 medical electrical environmental requirements and test methods GB/T 16886.1 Biological evaluation of medical devices - Part 1. Evaluation of the risk management process and Test Symbols - Part 1 YY/T 0466.1-2009 medical equipment used with medical device labels, labeling and information. General Claim YY 0505 Medical electrical equipment - Part 1-2. General requirements for safety Collateral standard. Electromagnetic compatibility requirements and tests YY 0607-2007 Medical electrical equipment - Part 2. nerve and muscle stimulation requirements for the safety Used YY 0868-2011 nerve and muscle stimulation electrodes

3 Terms and Definitions

GB 9706.1-2007 and YY 0607-2007 defined and the following terms and definitions apply to this document. 3.1 While more than two (including two) different IF frequencies (1000Hz ~ 100000Hz frequency within the range) AC current post Fork acts on the human body, in the low-frequency modulation current organization formed to an apparatus for treatment. 3.2 Difference frequency beatfrequency Difference in frequency between two carriers. 3.3 Carrier carrierwave A cyclical oscillating current. In the modulation wave, modulated frequency AC current. 3.4 Modulation modulation By modulating a carrier wave to change certain characteristics (e.g., amplitude, frequency or phase) of the process. 3.5 Dual interference two-pathinterference
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