Evaluation of pyrogens remaining on reusable medical devices after washing and sterilization

Author:

Nomura Yusuke1,Fukui Chie1,Yamamura Junji2,Kuromatsu Hisashi2,Naito Tomoko3,Takahashi Yuichi3,Haishima Yuji1

Affiliation:

1. 国立医薬品食品衛生研究所

2. 株式会社IHI

3. 浦工業株式会社

Publisher

Japanese Society of Medical Instrumentation

Subject

General Medicine

Reference20 articles.

1. 1) DGKH, DGSV, AKI. Validation and routine monitoring of automated cleaning and thermal disinfection processes for medical devices (5th Edition 2017), Zentral Sterilisation, Suppl. 2017.

2. 2) Guideline for evaluation and assessment of medical instrument cleanliness. Japanese Society of Medical Instrumentation, 2012.

3. 3) A compendium of processes, materials, test methods, and acceptance criteria for cleaning reusable medical devices. Technical information report. AMMI TIR30: 2011/(R) 2016.

4. 4) Rietschel ET, Brade L, Schade U, et al. “Chemical structure and biological activity of lipopolysaccharides”. Endotoxin from pathophysiology to therapeutic approaches. Baumgartner JD, Calandra T, Carlet J, ed. Paris: Flammarion Medicine-Sciences,1990, p. 5–18.

5. 5) Rietschel ET, Wollenweber HW, Zähringer U, et al. “Bacterial lipopolysaccharides and their lipid A component”. Bacterial endotoxin; Chemical, biological and clinical aspects. Homma JY, Kanegasaki S, Lüderitz O, et al ed. Weinheim: Wiley-VCH Verlag GmbH, 1984, p.11–22.

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