GB/T 48011-2026
具有组织密度差的可吸收生物材料 体内降解率测定 X射线显微CT法
Absorbable/resorbable biomaterials characterized by different density from surrounding tissue—Determination of the biodegradation in vivo—X-ray microCT test method
- 实施日期
- 2027-08-01
- ICS 分类
- 11.100.20
组合使用关键词、标准类型、状态与 ICS 分类,快速定位所需国家标准。
找到 167 条
GB/T 48011-2026
Absorbable/resorbable biomaterials characterized by different density from surrounding tissue—Determination of the biodegradation in vivo—X-ray microCT test method
GB/T 48010-2026
Single-use containers for the collection of specimens from humans other than blood
GB/T 47486-2026
General technical requirements for vasculature-on-a-chip
GB/Z 136-2026
Medical laboratories—Reagents for staining biological specimen—Guidance for users
GB/Z 157-2026
In vitro diagnostic test systems—Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods
GB/T 16886.2-2026
Biological evaluation of medical devices—Part 2: Animal welfare requirements
GB/T 46943-2025
Clinical laboratory testing and in vitro diagnostic test systems—General requirements for metagenomic next-generation sequencing validation
GB/T 46942.1-2025
Single-molecule gene sequencing—Part 1:Terminology
GB/T 46660-2025
General technical requirements for whole genome sequencing of SARS-CoV-2
GB/T 39367-2025
In vitro diagnostic test systems—Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens—Laboratory quality practice guide
GB/T 21771-2025
Chemicals—Test method of combined repeated dose toxicity study with the reproduction/developmental toxicity screening
GB/T 46302-2025
Automatic sample processing system for medical use
GB/T 46454-2025
Clinical laboratory testing and in vitro diagnostic test systems—Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
GB/T 16886.17-2025
Biological evaluation of medical devices—Part 17:Toxicological risk assessment of medical device constituents
GB/T 21415-2025
In vitro diagnostic medical devices—Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
GB/T 45214-2025
Data quality evaluation method of human whole genome sequencing
GB/T 44831-2024
General technical requirements of skin-on-a-chip
GB/T 44827-2024
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
GB/T 44467-2024
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for saliva—Isolated human DNA
GB/T 42080.3-2024
Molecular in vitro diagnostic examinations—Specifications for pre-examination processes for frozen tissue—Part 3: Isolated DNA