Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices | ANSI/AAMI/ISO 14937:2009/(R)2013; Sterilization
EN ISO 14937:2009 - Sterilization of health care products - General requirements for
Overview Standards | PDF | Medical Device | Sterilization (Microbiology)
ISO 14937 : Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
nopa instruments: Container: DIN ISO 14937 & DIN EN 868-8 certified
UNE-EN ISO 14937:2010
ISO 11135:2014
DIN EN ISO 14937
What is the level of treatment required for your endoscopes? - Steelco
AAMI/ISO 14937:2009/(R)2013
BS EN ISO 14937:2009
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STERIS VHP® LTS-V Low Temperature Sterilization - ISO 14937 Process Validation Services - YouTube
Esterilización de productos para el cuidado de la salud. requisitos generales para la caracterización de un agente esterilizante y para el desarrollo, la validación y el control de rutina de un proceso
ISO 14937:2009 - Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
ISO 14937:2000 - Sterilization of health care products -- General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
ISO 14937:2009 - Sterilization of health care products — General requirements for characterization
BS EN ISO 14937:2009 Sterilization of health care products. General requirements for characterization of a
DIN EN ISO 14937:2010 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical