GB 8368-2018 PDF in English
GB 8368-2018 (GB8368-2018) PDF English
| Standard ID | Contents [version] | USD | STEP2 | [PDF] delivered in | Name of Chinese Standard | Status |
| GB 8368-2018 | English | 225 |
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Infusion sets for single use -- Gravity feed
| Valid |
| GB 8368-2005 | English | 140 |
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Infusion sets for single use, gravity feed
| Obsolete |
| GB 8368-1998 | English | 719 |
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Infusion sets for single use
| Obsolete |
| GB 8368-1993 | English | RFQ |
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Infusion sets for single use
| Obsolete |
Standards related to (historical): GB 8368-2018
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GB 8368-2018: PDF in English GB 8368-2018
NATIONAL STANDARD OF THE
PEOPLE’S REPUBLIC OF CHINA
ICS 11.040.20
C 31
Replacing GB 8368-2005
Infusion sets for single use - Gravity feed
(ISO 8536-4:2010, Infusion equipment for medical use –
Part 4: Infusion sets for single use, gravity feed, MOD)
ISSUED ON: MARCH 15, 2018
IMPLEMENTED ON: APRIL 01, 2021
Issued by: General Administration of Quality Supervision, Inspection and
Quarantine of the PRC;
Standardization Administration of the PRC.
Table of Contents
Foreword ... 4
1 Scope ... 6
2 Normative references ... 6
3 General requirements ... 7
4 Designation ... 9
4.1 Infusion set ... 9
4.2 Air-inlet device ... 9
5 Materials ... 9
6 Physical requirements ... 10
6.1 Physical requirements ... 10
6.2 Leakage ... 10
6.3 Tensile strength ... 10
6.4 Closure-piercing device ... 10
6.5 Air-inlet device ... 11
6.6 Tubing ... 11
6.7 Fluid filter ... 11
6.8 Drip chamber and drip tube ... 11
6.9 Flow regulator ... 12
6.10 Flow rate of infusion fluid ... 12
6.11 Injection site ... 12
6.12 Male conical fitting ... 12
6.13 Protective caps ... 12
7 Chemical requirements ... 13
7.1 Reducing (oxidizable) matter ... 13
7.2 Metal ions ... 13
7.3 Titration acidity or alkalinity ... 13
7.4 Residue on evaporation ... 13
7.5 UV absorption of extract solution ... 13
7.6 Ethylene oxide residuals ... 13
8 Biological requirements ... 13
8.1 General ... 13
8.2 Sterility ... 14
8.3 Pyrogenicity ... 14
8.4 Haemolysis ... 14
8.5 Toxicity ... 14
9 Labelling ... 14
9.1 Unit container ... 14
9.2 Shelf or multi-unit container ... 15
10 Packaging ... 16
11 Disposal ... 16
Annex A (Normative) Physical tests ... 17
Annex B (Normative) Chemical tests ... 22
Annex C (Normative) Biological tests ... 24
Annex D (Informative) Guidelines for design and implementation ... 25
Annex E (Informative) Technical differences of this Standard and ISO 8536-
4:2010 and causes ... 30
Bibliography ... 33
Foreword
The full technical content of this Standard is mandatory.
This Standard is drafted in accordance with the rules given in GB/T 1.1-2009.
This Standard replaces GB 8368-2005 “Infusion sets for single use, gravity
feed”. Compared with GB 8368-2005, in addition to editorial changes, the main
technical changes of this Standard are as follows:
- CHANGE the note in Tubing to the text (see 6.6; 6.6 of the 2005 edition);
- Delete the limit on the colour of the flow regulator (6.9 of the 2005 edition);
- Modify the position requirement of injection site to mandatory requirement
and add a note (see 6.11; 6.11 of the 2005 edition);
- Modify the requirement of male conical fitting to mandatory requirement
(see 6.12; 6.12 of the 2005 edition);
- Modify the requirements for reducing matter and the method of presentation
of test method (see 7.1 and B.2; 7.1 and B.2 of the 2005 edition);
- In Labelling, add a requirement that the presence of substances of interest
can be indicated by using symbol 2725 of ISO 7000 (see notes to 9.1 and
9.2);
- ADD packaging requirement (see 10.3);
- ADD disposal requirement (see Clause 11);
- Modify particulate contamination index and its test method (see A.1; A.1 of
the 2005 edition);
- Modify tests for leakage (see A.2; A.2 of the 2005 edition).
This Standard uses the redraft law to modify and adopt ISO 8536-4:2010
“Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity
feed”.
There are technical differences between this Standard and ISO 8536-4:2010.
The clauses involved in these differences have been marked by a vertical single
line (|) at the blank of the outer margin. Annex E gives a list of the corresponding
technical differences and their causes.
This Standard incorporates the amendment contents of ISO 8356-
4:2010/Amd.1:2013. The clause-subclause involved in these amendment
contents has been marked by vertical double line (||) at the blank of the outer
margin.
This Standard also makes the following editorial changes:
- ADD the informative Annex D, to provide guidelines for the design and
implementation of infusion sets in China;
- ADD the informative Annex E, giving a list of corresponding technical
differences and their causes compared to ISO 8536-4:2010.
Attention is drawn to the possibility that some of the elements of this document
may be the subject of patent rights. The issuing authority of this document shall
not be held responsible for identifying any or all such patent rights.
This Standard was proposed by and shall be under the jurisdiction of China
Food and Drug Administration.
Main drafting organizations of this Standard: Shandong Quality Inspection
Center for Medical Devices, Shandong Weigao Group Medical Polymer Co.,
Ltd., Shinva Ande Healthcare Apparatus Co., Ltd., Shanghai Kindly Enterprise
Development Group Co., Ltd., Jiangxi Hongda Medical Equipment Group Ltd.,
Tianjin Hanaco Medical Co., Ltd., Jiangxi Sanxin Medtec Co., Ltd., Chengdu
Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd., Shandong
Zhongbaokang Medical Implements Co., Ltd.
Main drafters of this Standard: Wan Min, Wang Yi, Li Songhua, Pan Huaxian,
Gao Yicen, Wang Haiyin, Hou Li, Zhu Li, Liu Xiaohong, Tian Xinglong, Zhang
Min.
The previous editions of the standard replaced by this Standard were released
as follows:
- GB 8368-1987, GB 8368-1993, GB 8368-1998, GB 8368-2005.
Infusion sets for single use - Gravity feed
1 Scope
This Standard specifies the designation, materials, physical, chemical, and
biological requirements for single-use gravity feed infusion sets.
This Standard applies to single-use gravity feed infusion sets for use with
infusion containers and intravenous equipment.
2 Normative references
The following documents are indispensable for the application of this document.
For the dated references, only the editions with the dates indicated are
applicable to this document. For the undated references, the latest edition
(including all the amendments) are applicable to this document.
GB/T 1962.2 Conical fittings with a 6% (Luer) taper for syringes, needles and
certain other medical equipment - Part 2: Lock fittings (GB/T 1962.2-2001,
ISO 594-2:1998, IDT)
GB/T 6682 Water for analytical laboratory use - Specification and test
methods (GB/T 6682-2008, ISO 3696:1987, MOD)
GB/T 14233.1-2008 Test methods for infusion, transfusion, injection
equipment for medical use - Part 1: Chemical analysis methods
GB/T 14233.2 Test methods for infusion, transfusion, injection equipment for
medical use - Part 2: Biological test methods
GB 15811 Sterile hypodermic needles for single use (GB 15811-2016, ISO
7864:1993, NEQ)
GB/T 16886.1 Biological evaluation of medical devices - Part 1: Evaluation
and testing within a risk management process (GB/T 16886.1-2011, ISO
10993-1:2009, IDT)
GB/T 25915.1 Cleanrooms and associated controlled environments - Part 1:
Classification of air cleanliness (GB/T 25915.1-2010, ISO 14644-1:1999, IDT)
YY/T 0466.1 Medical devices - Symbols to be used with medical device
labels, labelling and information to be supplied - Part 1: General
requirements (YY/T 0466.1-2016, ISO 15223-1:2012, IDT)
3 General requirements
3.1 The nomenclature to be used for components of infusion sets and of a
separate air-inlet device is given in Figures 1, 2 and 3. These figures illustrate
examples of the configuration of infusion sets and air-inlet devices; other
configurations may be used provided they lead to the same results. Infusion
sets as illustrated in Figure 2 should only be used for collapsible plastic
containers. Infusion sets as illustrated in Figure 2 used with separate air-inlet
devices as illustrated in Figure 3, or infusion sets as illustrated in Figure 1, shall
be used for rigid containers.
3.2 The infusion set shall be provided with protective caps to maintain sterility
of the internal parts of the set until the set is used. The air-inlet device shall be
provided with a protective cap over the closure-piercing device or needle.
......
Source: Above contents are excerpted from the PDF -- translated/reviewed by: www.chinesestandard.net / Wayne Zheng et al.
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