KS P ISO 23640
체외 진단 의료기기 — 체외 진단 시약의 안정성 평가
体外诊断医疗器械 - 体外诊断试剂稳定性评估
2019-11-25
BS EN ISO 23640-2015
In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
体外诊断医疗设备 体外诊断试剂稳定性评价
2015-06-30
KS P ISO 23640(2024 Confirm)
체외 진단 의료기기 — 체외 진단 시약의 안정성 평가
体外诊断医疗器械——体外诊断试剂稳定性评价
2019-11-25
YY/T 1579-2018
体外诊断医疗器械 体外诊断试剂稳定性评价
In vitro diagnostic medical devices—Evaluation of stability of in vitro diagnostic reagents
2018-02-24
ISO 23640-2011
In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
体外诊断医疗器械——体外诊断试剂稳定性评价
2011-11-29
UNE-EN 13640-2002
Stability testing of in vitro diagnostic reagents.
体外诊断试剂的稳定性试验
2002-07-29
GOST R ISO 23640-2015
Изделия медицинские для диагностики in vitro. Оценка стабильности реагентов для диагностики in vitro
体外医疗器械 评估体外诊断试剂的稳定性
GB/T 26124-2011
临床化学体外诊断试剂(盒)
In vitro diagnostic reagent(kit) for clinical chemistry
2011-05-12
UNE-EN 12376-1999
IN VITRO DIAGNOSTIC MEDICAL DEVICES. INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR STAINING IN BIOLOGY.
体外诊断医疗设备 制造商提供的用于生物学染色的体外诊断试剂的信息
1999-07-20
BS EN ISO 19001-2013
In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
体外诊断医疗设备 制造商提供的用于生物学染色的体外诊断试剂的信息
2013-08-31
DIN EN 12376
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
体外诊断医疗器械——制造商提供的用于生物学染色的体外诊断试剂的信息；德文版EN 12376:1999
1999-04-01
YY/T 0639-2019
体外诊断医疗器械 制造商为生物学染色用体外诊断试剂提供的信息
In vitro diagnostic medical devices—Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
2019-07-24
ISO 19001-2013
In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
体外诊断医疗器械——制造商提供的用于生物学染色的体外诊断试剂的信息
2013-03-07
BS EN ISO 18113-2-2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for professional use
体外诊断医疗设备 制造商提供的信息（标签）
2012-01-31
BS EN ISO 18113-4-2011
In vitro diagnostic medical Devices. Information supplied by the manufacturer (labelling)-In vitro diagnostic reagents for self-testing
体外诊断医疗设备 制造商提供的信息（标签）
2012-01-31
GOST R ISO 19001-2021
Медицинские изделия для диагностики in vitro. Информация, предоставляемая изготовителем с диагностическими реагентами in vitro, применяемыми для окрашивания биологических материалов
体外诊断医疗设备 制造商提供的关于生物材料染色用体外诊断试剂的信息
YY/T 1227-2014
临床化学体外诊断试剂(盒)命名
In vitro diagnostic reagent(kit)nomenclature for clinical chemistry
2014-06-17
GB/T 29791.4-2013
体外诊断医疗器械 制造商提供的信息(标示) 第4部分:自测用体外诊断试剂
In vitro diagnostic medical devices—Information supplied by the manufacturer (labelling)—Part 4:In vitro diagnostic reagents for selftesting
2013-10-10
UNE-EN 376-2002
Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing.
制造商提供的用于自检的体外诊断试剂信息
2002-06-27
UNE-EN 375-2001
INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR PROFESSIONAL USE.
由制造商提供的供专业使用的体外诊断试剂信息
2001-07-27