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US$189.00 · In stock Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. YY/T 1245-2014: Automatic blood grouping analyzer Status: Valid
| Standard ID | Contents [version] | USD | STEP2 | [PDF] delivered in | Standard Title (Description) | Status | PDF |
| YY/T 1245-2014 | English | 189 |
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Automatic blood grouping analyzer
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YY/T 1245-2014
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Basic data | Standard ID | YY/T 1245-2014 (YY/T1245-2014) | | Description (Translated English) | Automatic blood grouping analyzer | | Sector / Industry | Medical Device & Pharmaceutical Industry Standard (Recommended) | | Classification of Chinese Standard | C44 | | Classification of International Standard | 11.100 | | Word Count Estimation | 8,869 | | Date of Issue | 6/17/2014 | | Date of Implementation | 7/1/2015 | | Quoted Standard | GB/T 191; GB 4793.1; GB/T 14710; YY/T 0466.1; YY 0648 | | Regulation (derived from) | China Food and Drug Administration in 2014 Bulletin No. 30 | | Issuing agency(ies) | State Food and Drug Administration | | Summary | This Standard applies to the human red blood cell blood grouping, antibody screening tests, such as column agglutination, microplate method automatic blood analyzer. This Standard specifies requirements for automatic blood analyzer, test methods, labeling |
YY/T 1245-2014: Automatic blood grouping analyzer---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.
Automatic blood grouping analyzer
ICS 11.100
C44
People's Republic of China pharmaceutical industry standards
Automatic blood analyzer
Issued on. 2014-06-17
2015-07-01 implementation
China Food and Drug Administration released
Foreword
This standard was drafted in accordance with GB/T 1.1-2009 given rules.
Please note that some of the content of this document may involve patents. Distribution of this document
Institutions do not assume the responsibility to identify these patents.
This standard was proposed by the China Food and Drug Administration.
This standard by the national medical clinical laboratory testing and in vitro diagnostic systems for Standardization Technical Committee (SAC/TC136) centralized.
This standard was drafted. Beijing Medical Device Testing, Beckman Coulter Trading (China) Co., Ltd., Shenzhen Electronics Icahn has
Limited, Johnson & Johnson (Shanghai) Medical Equipment Co., Ltd.
The main drafters of this standard. Bi Chunlei, He Xueying, Zhang Jinwen, BIMONTHLY Nie Jing.
Automatic blood analyzer
1 Scope
This standard specifies requirements for automatic blood analyzer, test methods, labeling and instructions for use, packaging, transportation and storage.
This standard applies to the human red blood cell blood grouping, antibody screening test and other automatic blood analyzer (hereinafter referred to as the analyzer).
This standard specifies only the column agglutination method, a method microplate blood analysis instrument technical requirements.
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 Packaging - Pictorial signs
GB 4793.1 measurement, control and laboratory safety requirements for electrical equipment - Part 1. General requirements
GB/T 14710 medical electrical environmental requirements and test methods
Symbols - Part 1 YY/T 0466.1 medical equipment used with medical device labels, labeling and information. General requirements
YY 0648 measurement, control and laboratory safety requirements for electrical equipment - Part 2-101. In vitro diagnostic (IVD) medical equipment
Special requirements
3 Requirements
3.1 blood typing accuracy
3.1.1 ABO blood group determination system
Blood samples were seized, agglutination reaction with the corresponding private positive stereotypes and counter-stereotypes reagents, the analyzer shall automatically report the correct
ABO typing results.
3.1.2 Rh blood group determination
After blood samples were seized, with the corresponding dedicated reagent agglutinate, the analyzer shall automatically reports the correct Rh (D) negative and positive
result.
Stability Analyzer 3.2
After boot 30min, 8h, detected by the analyzer known blood sample, the test results should be consistent with the known results.
3.3 Temperature Control
Incubation temperature should be set within ± 2.0 ℃ temperature range.
3.4 centrifuge speed
Working speed conditions, the test speed deviation should be ± 2.5% within the range set value.
NOTE. This applies to the use of centrifugal method analyzer.
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