1. Guidance for Industry and for FDA Staff: Enforcement Priorities for Single-Use Devices Reprocessed by Third Parties and Hospitals;United States Food and Drug Administration
2. United States Food and Drug Administration. Draft Guidance for Industry and FDA Staff: Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling, Draft Document Issued on 2 May 2011. Latest Edition Issued on 9 June 2017.
3. Hygiene requirements for the reprocessing of medical devices. Recommendation of the commission for hospital Hygiene and infection Prevention (KRINKO) at the Robert Koch Institute (RKI) and the Federal Institute for Drugs and Medical Devices (BfArM);Commission for Hospital Hygiene and Infection Prevention (KRINKO) & Federal Institute for Drugs and Medical Devices (BfArM);Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz,2012
4. Points to Consider for the Reprocessing of Single-Use Devices: Co-signed Notification of the Managers of the Evaluation and Licensing Division(0731-No. 8), the Pharmaceutical Safety Division (0731-No. 5), and the Compliance and Narcotics Division and Safety (0731-No. 1);Ministry of Health, Labour and Welfare
5. Ministry of Health, Labour and Welfare. Points to Consider for Writing an Application for Marketing Authorisation for the Reprocessing of Single-Use Devices, Co-signed Notification of the Managers of the Evaluation and Licensing Division(0816-No. 3), Ministry of Health, Labour and Welfare. Issued on 16 August 2017.