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GB 11244-2005

GB 11244-2005_English: PDF (GB11244-2005)
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GB 11244-2005English105 Add to Cart 0--3 minutes. Auto-delivered. General requirements for the medical endoscope and endoscope accessories GB 11244-2005 Obsolete GB 11244-2005

BASIC DATA
Standard ID GB 11244-2005 (GB11244-2005)
Description (Translated English) General requirements for the medical endoscope and endoscope accessories
Sector / Industry National Standard
Classification of Chinese Standard C40
Classification of International Standard 11.040.55
Word Count Estimation 12,114
Date of Issue 2005-07-21
Date of Implementation 2005-12-01
Older Standard (superseded by this standard) GB 11244-1989
Quoted Standard GB/T 191-2000; GB 9706.19-2000; GB/T 14710-1993; GB/T 16886.1-2001
Adopted Standard ISO 8600-1997, NEQ; DIN 58105, IDT
Drafting Organization Shanghai Medical Optical Instrument Factory
Administrative Organization National Medical optics and instruments Standardization Technical Committee
Regulation (derived from) Announcement of Newly Approved National Standards No. 10 of 2005 (No. 84 overall)
Proposing organization State Food and Drug Administration
Issuing agency(ies) General Administration of Quality Supervision, Inspection and Quarantine of the People Republic of China, China National Standardization Administration Committee
Summary This Chinese standard gives the clinical use of medical endoscopes and endoscopic accessories terminology, general technical requirements, general test methods, inspection rules, marking, instructions, packaging, transportation and storage. Various types of endoscopes dedicated technical requirements should conform to specific standards.

GB 11244-2005
GB
NATIONAL STANDARD OF THE
PEOPLE’S REPUBLIC OF CHINA
ICS 11.040.55
C 40
Replacing GB 11244-1989
General requirements for the medical endoscope and
endoscope accessories
ISSUED ON: JULY 21, 2005
IMPLEMENTED ON: DECEMBER 01, 2005
Issued by: General Administration of Quality Supervision, Inspection and
Quarantine of the PRC;
Standardization Administration of the PRC.
Table of Contents
Foreword ... 3 
1 Scope ... 4 
2 Normative references ... 4 
3 Terms and definitions ... 4 
4 Requirements ... 8 
5 Type inspection ... 10 
6 Inspection rules ... 17 
7 Marking ... 18 
8 Instructions for use ... 18 
9 Packaging, transportation and storage ... 20 
General requirements for the medical endoscope and
endoscope accessories
1 Scope
This Standard gives the terminology, general technical requirements, general
test methods, inspection rules, marking, instructions for use, packaging,
transportation and storage of endoscope and endoscope accessories used in
medical clinics. The particular technical requirements for various types of
endoscopes shall meet the requirements of the corresponding particular
standards.
2 Normative references
The following documents contain provisions which, through reference in this
Standard, constitute provisions of this Standard. For the dated references, their
subsequent amendments (excluding corrections) or revisions do not apply to
this Standard. However, the parties who enter into agreement based on this
Standard are encouraged to investigate whether the latest editions of these
documents are applicable. For undated reference documents, the latest
editions apply to this Standard.
GB/T 191-2000 Packaging - Pictorial marking for handling of goods
GB 9706.19-2000 Medical electrical equipment - Part 2: Particular
requirements for the safety of endoscopic equipment (idt IEC 60601-2-
18:1996)
GB/T 14710-1993 The environmental requirements and test methods for
medical electrical equipment
GB/T 16886.1-2001 Biological evaluation of medical devices - Part 1:
Evaluation and testing (idt ISO 10993-1:1997)
3 Terms and definitions
The following terms and definitions apply to this Standard.
3.1
Endoscope
Where:
μ - The perimeter of the section, in millimeters (mm).
3.6
Distal
The position of the endoscope accessories of all endoscopes is farther from the
user than other reference points.
3.7
Proximal
The positions of all endoscopes and endoscope accessories are closer to the
user than other reference points.
3.8
Instrument channel
The part of an endoscope or endoscope accessory, which allows the
endoscope or endoscope accessory to pass through.
3.9
Insertion portion
The part of an endoscope or an endoscope accessory, which can be inserted
into a natural or surgically opened pore of the human body, or inserted into an
instrument channel of an endoscope or an endoscope accessory.
3.10
Maximum insertion portion width
The maximum external width of the full length of the insertion portion of the
endoscope or endoscope accessory.
3.11
Minimum insertion channel width
The minimum internal width of instrument channel.
3.12
Working length
4 Requirements
4.1 Surface and edge
4.1.1 Endoscopes and endoscope accessories shall be designed to not cause
any accidental harm to the human body.
4.1.2 All surfaces of the endoscope and endoscope accessories must not have
pores, cracks and burrs.
4.2 Maximum insertion portion width
The maximum insertion portion width must not be larger than the size specified
in the instructions for use provided by the manufacturer. See 8.2 c).
4.3 Minimum insertion channel width
The minimum insertion channel width must not be less than the size specified
in the instructions for use provided by the manufacturer. See 8.2 h).
4.4 Field of view
If the manufacturer has no other special regulations, the deviation of the field of
view of optical endoscope from the nominal value provided by the manufacturer
shall not exceed 15%. In the product catalog and manual materials, the
description of the field of view is not mandatory.
4.5 Direction of view
If the manufacturer has no other special regulations, the deviation of the
direction of view of optical rigid endoscope from the nominal value provided by
the manufacturer shall not exceed 10%.
4.6 Funnel-shaped eyepiece cover
The shape and size of funnel-shaped eyepiece cover shall be designed
according to Figure 3. In this way, the eyepiece can be connected to the
interfaces of cameras, movie cameras and video cameras produced by many
manufacturers.
5.2.3 Accuracy of measuring instrument
An instrument with an accuracy of 0.05 mm (such as vernier calipers) shall be
used for measurement. If the French size of the perimeter is measured, an
instrument with an accuracy of 0.5 mm (such as a tape measure or similar
measuring tool) shall be used.
5.2.4 Measurement process
5.2.4.1 Readings in millimeters
For the measurement of readings in millimeters, it shall measure the maximum
diameter of the circumscribed circle perpendicular to the axis of the insertion
portion [see Figure 4a) and b)]. This maximum diameter is defined as the
maximum diameter measured on all cross-sections perpendicular to the axis
along the entire length of the insertion portion.
For flexible endoscopes, the insertion portion shall be placed flat for
measurement.
To obtain a millimeter reading:
a) MEASURE the maximum diameter of the circumcircle.
b) If the endoscope uses a detachable cannula, under two conditions of
taking on and taking off cannula, the maximum diameter of the endoscope
shall be measured [see Figure 4a) and b)].
c) The unit of measurement is mm.
5.2.4.2 Readings in French size
For readings expressed in French size, it shall measure the maximum perimeter
of the cross-section perpendicular to the axis of the insertion portion. The
maximum perimeter is defined as the longest perimeter measured across all
cross-sections perpendicular to the axis along the entire length of the insertion
portion.
For flexible endoscopes, the insertion portion shall be placed flat for
measurement.
To obtain a French value:
a) If the cross-section of the insertion portion is circular, the French size can
be calculated by multiplying the measured diameter by 3.
b) If the cross-section of the insertion portion is non-circular (see Figure 5),
5.4 Field of view and direction of view
5.4.1 Measurement accuracy of field of view
The minimum allowable accuracy of measuring the field of view:
a) ±5% of the reading of rigid endoscope;
b) ±10% of the reading of flexible endoscope.
5.4.2 Measurement accuracy of direction of view
The minimum allowable accuracy of measuring the direction of view:
a) ±3° for rigid endoscope;
b) ±10° for flexible endoscope.
5.4.3 Measuring instrument
5.4.3.1 Optical bench, or similar equipment. It can support the optical
endoscope for testing; can adjust the central axis of the field of view to coincide
with the center of the measuring mark. In the vertical direction, the end face of
endoscope lens measures the field of view, at a distance of 50 from the
measuring mark center point of the concentric circle marked with an angle.
5.4.3.2 Target holder and dial divided by "degrees" (see Figure 6).
6.4 Determination rule and reinspection rule
6.4.1 The exit-factory inspection is a full inspection. If any of the inspection
items is not met, the product is not qualified.
6.4.2 Type inspection randomly selects 2 sets from the products, which have
passed the exit-factory inspection. For items with unqualified inspection results,
it is allowed to take double number of samples for reinspection of unqualified
items. If the reinspection is qualified, the product is deemed qualified. If the
reinspection is unqualified, then the product is deemed unqualified.
7 Marking
7.1 Least marking
Each endoscope and endoscope accessory shall have the following markings:
a) Trademark or other marks indicating the equipment and its manufacturer;
b) Maximum insertion portion width, minimum insertion channel width,
working length, field of view, and direction of view. The above marks are
necessary for the use of endoscopes and endoscope accessories. The
unit of the width of insertion portion and the width of instrument channel is
millimeters (mm). They can also be marked according to the French size
defined in 3.5, indicated by Fr or perimeter value;
c) Whether it is habitual or for some reason, the number of equipment and
disassembled parts or semi-disassembled parts shall be indicated in the
total or series number.
7.2 Clear marking
After the equipment is used, cleaned, disinfected, sterilized and stored in
accordance with the manufacturer's instructions for use, the markings must be
kept clear.
7.3 Exceptional marking
When it is impossible to mark on the separable part or the installation parts of
the separable part of the equipment due to the size or shape, the required mark
shall be partly marked on the package or partly on the instructions for use.
8 Instructions for use
8.1 The manufacturers of endoscopes and endoscope accessories provide
f) User replaceable parts and replacement instructions;
g) Where the user can get the professional services of the equipment;
h) Minimum insertion channel width of each equipment.
8.3 The prevention and application instructions when using the equipment shall
include:
a) Liquids suitable and unsuitable for endoscopes, such as control liquid,
sclerotherapy liquid, lubricants and anesthetics, and warnings for liquid
use;
b) Warning for the use of flammable gases.
9 Packaging, transportation and storage
9.1 There shall be the following markings on the outer packaging box:
a) Name and address of manufacturer;
b) Product name and model;
c) Product standard number;
d) Product registration number;
e) Volume (length×width×height);
f) Gross mass and net mass;
g) Exit-factory year and month;
h) There shall be signs such as "fragile article", "rain-proof", and "upward" in
accordance with GB/T 191-2000.
9.2 Each set of medical endoscopes and endoscope accessories shall be
accompanied by a product manual, inspection conformity certificate and
packing list; packaged in moisture-proof paper bags or plastic bags, and placed
in the box.
9.3 Medical endoscopes and endoscope accessories are first packed in a dry
shock-proof and moisture-proof box; and then packed into a shock-proof and
moisture-proof outer packaging box.
9.4 The transportation requirements are in accordance with the order contract.