
【国际标准】 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
本网站 发布时间:
2024-05-11
开通会员免费在线看70000余条国内标准,赠送文本下载次数,单本最低仅合13.3元!还可享标准出版进度查询、定制跟踪推送、标准查新等超多特权!  
查看详情>>

适用范围:
暂无
标准号:
ISO 18113-3:2022 EN
标准名称:
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
英文名称:
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use标准状态:
现行-
发布日期:
2022-10-06 -
实施日期:
出版语种:
EN
- 其它标准
- 上一篇: ISO 18113-3:2009 EN 0bca3837 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
- 下一篇: ISO 18113-4:2009 EN 0cbe9a1e In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
- 推荐标准
- ISO 13079:2011 EN eadd1f97 Laboratory glass and plastics ware — Tubes for the measurement of the erythrocyte sedimentation rate by the Westergren method
- ISO 15193:2009 EN 5d8f674f In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures
- ISO 15194:2009 EN 3a04baec In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation
- ISO 15197:2013 EN 8a967db0 In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
- ISO 16256:2021 EN dfaa6a07 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
- ISO 17511:2020 EN c5ed4ccf In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples
- ISO 18113-1:2022 EN 4c9101f2 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
- ISO 18113-3:2022 EN 9977c669 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
- ISO 18153:2003 EN 123e51a0 In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materials
- ISO 20166-4:2021 EN c96cd86f Molecular in vitro diagnostic examinations — Specifications for preexamination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 4: In situ detection techniques
- ISO 20184-1:2018 EN d3cace33 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 1: Isolated RNA
- ISO 20184-2:2018 EN aeec44bc Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 2: Isolated proteins
- ISO 23640:2011 EN 9afa3f35 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
- ISO 4307:2021 EN c9ef3494 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for saliva — Isolated human DNA
- ISO 6717:2021 EN 36dba182 In vitro diagnostic medical devices — Single-use containers for the collection of specimens from humans other than blood