GA/T 2340-2025 Active Industry standards-Public safety

GA/T 2340-2025 Rapid forensic DNA analysis system

Publish Date: 2025-04-14 Implement Date: 2025-09-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

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Basic Information

Standard Code: GA/T 2340-2025

Standard Type: Industry standards

Standard Status: Active

is_force_gb: no

CCS Name: Crime identification techniques

ICS Name: -

Publish Date: 2025-04-14

Implement Date: 2025-09-01

Pages: 16 pages

Scope

This document specifies the detection conditions, technical requirements, marking, packaging, transportation, storage, etc. of forensic DNA rapid detection equipment, describes the testing methods of forensic DNA rapid detection equipment, and establishes the inspection rules for key technical indicators.
This document is applicable to the manufacture, inspection, and application of fully integrated, automated forensic DNA detection equipment that integrates sample pretreatment, multiple PCR amplification, and capillary electrophoresis detection in non-laboratory environments.

Development Information

Word Count: 19 Thousand words Pages: 16 pages

Referenced Standards

GB/T 191-2008 Packaging—Pictorial marking for handling of goods GB/T 14710-2009 Environmental requirement and test methods for medical electrical equipment GB/T 18268.26-2010 Electrical equipment for measurement,control and laboratory use—EMC requirements—Part 26:Particular requirements—In vitro diagnostic (IVD) medical equipment GB/T 37226-2018 Criterion of forensic science human fluorescence STR multiplex amplification reagent GB/T 42125.14-2023 Safety requirements for electrical equipment for measurement,control and laboratory use—Part 14:Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes GA/T 1380-2018 Forensic science—Specifications for collection of human samples of DNA database JTG B01-2014 YY 0648-2008 Safety requirements for electrical equipment for measurement,control and laboratory use—Part 2-101:Particular requirements for in vitro diagnostic (IVD) medical equipment

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