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YY/T 1214-2013

Chinese Standard: 'YY/T 1214-2013'
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YY/T 1214-2013English150 Add to Cart 0--10 minutes. Auto immediate delivery. Human chorionic gonadotrophin quantitative labelling immunoassay kit Obsolete YY/T 1214-2013
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BASIC DATA
Standard ID YY/T 1214-2013 (YY/T1214-2013)
Description (Translated English) Human chorionic gonadotrophin quantitative labelling immunoassay kit
Sector / Industry Medical Device & Pharmaceutical Industry Standard (Recommended)
Classification of Chinese Standard C44
Classification of International Standard 11.100
Word Count Estimation 9,920
Quoted Standard YY/T 0466.1
Drafting Organization Chinese Academy of Food and Drug Testing
Administrative Organization National Medical clinical testing laboratories and in vitro diagnostic systems for Standardization Technical Committee
Regulation (derived from) State Food and Drug Administration Notice No. 36 of 2013; industry standard for filing Notice 2013 No. 12 (No. 168 overall)
Proposing organization State Food and Drug Administration
Issuing agency(ies) State Food and Drug Administration
Summary This standard specifies: a quantitative marker of human chorionic gonadotropin immunoassay kit classification, requirements, test methods, marking, labeling and instructions for use, packaging, transportation and storage. This standard applies to: the pri

YY/T 1214-2013 
YY
ICS 11.100
C 44
PHARMACEUTICAL INDUSTRY STANDARD
OF THE PEOPLE’S REPUBLIC OF CHINA
Human chorionic gonadotrophin quantitative labelling
immunoassay kit
人绒毛膜促性腺激素定量标记免疫分析试剂盒
ISSUED ON. OCTOBER 21, 2013
IMPLEMENTED ON. OCTOBER 1, 2014
Issued by. State Food and Drug Administration
Table of Contents
Foreword ... 3 
1  Scope ... 4 
2  Normative references ... 4 
3  Classifications ... 4 
4  Requirements ... 5 
5  Test methods ... 7 
6  Marks, labels and instructions ... 9 
7  Packaging, transportation and storage ... 10 
Bibliography ... 11 
Foreword
This Standard is drafted according to the rules specified in GB/T 1.1-2009.
Please note that some contents of this Standard may involve patents. The issuing
authority of this Standard does not undertake the responsibility of identifying these
patents.
The Standard was proposed by China Food and Drug Administration.
The Standard shall be under the jurisdiction of National Technical Committee on System
of Medical Clinical Test Lab and in Vitro Diagnostic System of Standardization
Administration of China.
Drafting organization of this Standard. National Institutes for Food and Drug Control.
The main drafters of this Standard. Huang Ying, Shen Shu, Zhang Chuntao, Yu Ting, and
Gao Shangxian.
Human chorionic gonadotrophin quantitative labelling
immunoassay kit
1 Scope
This Standard specifies the classification, requirements, test method, marks, labels,
operating instructions, packaging, transportation, and storage of the human chorionic
gonadotrophin quantitative labelling immunoassay kit.
This Standard is applicable to the quantitative detection of human chorionic gonadotrophin
(HCG) quantitative labelling immunoassay kit [herein after referred to as “HCG reagent
(kit)”] that is based on the principle of double antibody sandwich method. It includes the
HCG immunoassay kit for quantitative detection by using labelling methods such as
enzyme labelling, (electrical) chemiluminescent labelling, (time resolution) fluorescence
AS capture antibody; and using microplates, pipes, magnetic particles, microbeads and
plastic beads and others AS the carrier coated antibody.
The Standard does not apply to.
a) Colloidal gold labelled HCG test strip;
b) Various types of HCG radio-immunity or IRMA reagent kit labelled with 125I and other
radioactive isotopes.
2 Normative references
The articles contained in the following documents have become part of this document
when they are quoted herein. For the dated documents so quoted, all the modifications
(including all corrections) or revisions made thereafter shall be applicable to this
document.
YY/T 0466.1-2009 Medical devices - Symbols to be used with medical device labels,
labelling and information to be supplied - Part 1. General requirements
3 Classifications
The HCG reagent kit can be classified into enzyme labelling HCG reagent kit, (electrical)
chemiluminescent labelling HCG reagent kit, (time resolution) fluorescence labelling HCG
reagent kit etc., according to the various labelling methods. It can also be divided into
different kinds of HCG reagent with carriers microplates, pipes, magnetic particles,
6 Marks, labels and instructions
6.1 Outer package of reagent (kit)
The marks and labels of the kit’s outer packaging box shall comply with the provisions of
YY/T 0466.1, and at least contain the following contents.
a) Product name and specifications;
b) Name, address and contact information of manufacturing enterprise;
c) Medical device registration certificate number and product standard number;
d) Product batch number;
e) Period of validity;
f) Storage conditions.
6.2 Label of each component of reagent (kit)
It shall contain at least the following contents.
a) Product name and specifications;
b) Name or marks of manufacturing enterprise;
c) Product batch number;
d) Period of validity;
e) Storage conditions.
6.3 Operating instructions of reagent (kit)
It shall generally contain the following contents.
a) Product name;
b) Packaging specifications;
c) Intended use;
d) Inspection principle;
e) Main compositions;
f) Storage conditions and period of validity;
Bibliography
[1] GB/T 3358.1 Statistical terminology - Part 1. General statistical terms and terms used
in probability
[2] JJF 1001-2011 General Terms in Metrology and Their Definitions
[3] Ye Yingwu. National Guide to Cl......
Related standard:   YY/T 1214-2019  YY/T 1213-2019
Related PDF sample:   YY/T 1213-2013  YY/T 1216-2013
   
 
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