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YY/T 0619-2017

Chinese Standard: 'YY/T 0619-2017'
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YY/T 0619-2017English150 Add to Cart 0--10 minutes. Auto immediate delivery. Medical endoscopes--Rigid resectosocope Valid YY/T 0619-2017
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BASIC DATA
Standard ID YY/T 0619-2017 (YY/T0619-2017)
Description (Translated English) Medical endoscopes--Rigid resectosocope
Sector / Industry Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard C40
Classification of International Standard 11.040.99
Word Count Estimation 10,131
Date of Issue 2017-02-28
Date of Implementation 2018-01-01
Older Standard (superseded by this standard) YY 0619-2007
Drafting Organization Zhejiang Medical Device Inspection Institute, Hangzhou good grams Photoelectric Instrument Co., Ltd., Shenyang Shen large endoscope Co., Ltd.
Administrative Organization National Medical Optics and Instrumentation Standardization Technical Committee (SAC/TC 103/SC 1)
Proposing organization China Food and Drug Administration
Issuing agency(ies) State Food and Drug Administration

YY/T 0619-2017
YY
PHARMACEUTICAL INDUSTRY STANDARD
OF THE PEOPLE’S REPUBLIC OF CHINA
ICS 11.040.99
C 40
Replacing YY 0619-2007
Medical Endoscopes – Rigid Resectoscope
医用内窥镜 硬性电凝电切内窥镜
ISSUED ON. FEBRUARY 28, 2017
IMPLEMENTED ON. JANUARY 01, 2018
Issued by. China Food and Drug Administration
Table of Contents
Foreword ... 3
1 Scope ... 5
2 Normative References ... 5
3 Classification and Composition ... 6
4 Requirements ... 6
5 Test Methods ... 11
Medical Endoscopes – Rigid Resectoscope
1 Scope
This Standard specifies the classification and composition, requirements and test
methods of rigid resectoscope.
This Standard is applicable to the rigid resectoscope (hereinafter referred to as
resectoscope). The resectoscope is clinically applicable to the cutting, vaporizing and
coagulating operations against the diseased tissues under the direct viewing of
endoscope and using the high-frequency current thermal effect.
2 Normative References
The following documents are essential to the application of this document. For the
dated documents, only the versions with the dates indicated are applicable to this
document; for the undated documents, only the latest version (including all the
amendments) are applicable to this document.
GB 9706.4 Medical Electrical Equipment - Part 2-2. Particular Requirements for
the Safety of High Frequency Surgical Equipment
GB 9706.19 Medical Electrical Equipment-Part 2. Particular Requirements for the
Safety of Endoscopic Equipment
GB/T 14233.1-2008 Test Methods for Infusion Transfusion Injection Equipment for
Medical Use - Part 1. Chemical Analysis Methods
GB/T 16886.1 Biological Evaluation of Medical Devices - Part 1. Evaluation and
Testing Within a Risk Management Process
YY 0068.1-2008 Medical Endoscopes - Rigid Endoscope - Part 1. Optical
Properties and Test Methods
YY 0068.2-2008 Medical Endoscopes - Rigid Endoscope – Part 2. Mechanical
Properties and Test Methods
YY 0068.3-2008 Medical Endoscopes - Rigid Endoscope – Part 3. Marking and
Instruction Manual
possible measures to minimize the undesired hazard. All the adopted measures shall
at least include the following instructions in the attaching document.
a) Warn the possible hazard indications, means of prevention of hazard, and the
handling instructions after hazard is discovered;
b) Safe operating procedures;
c) The instructions that can be used by the operator after special training.
4.2.2.6.2 In the view filed of the endoscope, the visible head end part of the surgical
electrode shall have no directional reflection phenomenon that may influence the use.
4.2.2.7 Visibility of surgical electrode
When the surgical electrode is moved to the distal position with the moving part of the
manipulator, its head end shall be within the range observable by the endoscope
4.3 Conduction performance
The high-frequency connection wire and surgical electrode of resectoscope shall be
well-conducted; its impedance value shall be less than 3Ω.
4.4 Label and attaching document
4.4.1 General requirements of label and attaching document
It shall meet the requirements of YY 0068.3-2009.
4.4.2 Other requirements of label and attaching document
The manufacturer shall indicate in the instruction manual the possibility of heat and
other risks to the patient and operator when using the product.
a) Thermal damage to the endoscope due to electrical spark or capacitively coupling
high-frequency current;
b) Image interference on the video screen caused by high-frequency
electromagnetic waves;
c) Keep the working part of the charged electrode within the operator’s observation
range to avoid accidental high-frequency burns;
d) In order to ensure that the charged electrode in the correct position during the
operation, it must be kept sufficient distance away from the head end of the
endoscope; it shall avoid contacting with the metal parts and other conductors of
the endoscope before exciting the high-frequency output, including the liquid
vent that may be conductor;
application; or information about the material and/or device is otherwise available, and the
material has been previously proven to be applicable.
NOTE2. If metallic material uses the medical metallic material suitable for the application range
of the national and industry standards, biological test may not be repeated.
4.5.4 Dissolved precipitates of polymer materials in contact with the patient
4.5.4.1 pH. compared with the same batch of blank control solution, the pH difference
shall be no greater than 2.0.
4.5.4.2 Total content of soluble heavy metals. the total content of the soluble heavy
metals in the dissolution solution shall not exceed 5.0µg/mL.
4.5.4.3 Potassium permanganate reducing substance. the consumption difference with
the same volume of the same batch of blank control solution shall be no more than
2.0mL.
4.6 Corrosion resistance (applicable to the non-disposable products)
The martensitic and austenitic stainless-steel materials are tested as per the boiling
water test method specified in YY/T 0149-2006, which shall meet the requirements of
Class-b; the remaining materials shall be performed once disinfection and sterilization
method that is most unfavorable for the device specified by the manufacturer in the
instruction manual, which shall meet the requirements of Class-b.
4.7 Disinfection and sterilization
4.7.1 Resistance of the re-disinfected and re-sterilized products
It shall meet the requirements of YY 0068.4-2009.
4.7.2 Sterile supply product
It shall meet the requirements of YY 0068.4-2009.
4.8 Package
It shall meet the requirements of YY 0068.4-2009.
4.9 Electrical safety performance
4.9.1 The electrical safety performance requirements of endoscope shall meet the
requirements of YY 0068.4-2009.
4.9.2 The electrical safety performance requirements of surgical electrode shall meet
the requirements of GB 9706.4.
5.5.2 Material quality requirement test
The main structure of the polymer material shall be confirmed by verification data
provided by the manufacturer.
Chemical composition test of the metallic material. take the method with accuracy
greater than or reaching the tolerance or 1/3 limit value to carry out the chemical
composition analysist test of the material.
5.5.3 Biocompatibility test
All tests are preferred to use the relevant standards of GB/T 16886 and perform the
test as per their methods.
5.5.4 Test on the dissolved precipitate of polymer material in contract with
patient
5.5.4.1 Preparation of test solution. prepare according to the sixth method in Table 1
of GB/T 14233.1-2008.
5.5.4.2 pH. follow the method specified in 5.4.1 of GB/T 14233.1-2008.
5.5.4.3 Heavy metal. follow the method specified in 5.6 of GB/T 14233.1-2008.
5.5.4.4 Potassium permanganate reducing substance. follow the method specified in
5.2 of GB/T 14233.1-2008.
5.6 Corrosion resistance (applicable to the non-disposable products) test
The martensi......
Related standard:   YY/T 0719.8-2019  YY 0290.3-2018
Related PDF sample:   YY 0762-2017
   
 
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