Home

iso 14937

BS EN ISO 14937:2009 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的一般要求标准
BS EN ISO 14937:2009 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的一般要求标准

DIN EN ISO 14937
DIN EN ISO 14937

Manufacturing / Monitoring
Manufacturing / Monitoring

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 14937:2009 - 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

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
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

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 14937:2000 - 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

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
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

ISO 14937 Health Care Sterilization
ISO 14937 Health Care Sterilization

ANSI/AAMI/ISO 14937:2009/(R)2013; 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 | Semantic
ANSI/AAMI/ISO 14937:2009/(R)2013; 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 | Semantic

ISO 14937
ISO 14937

STERIS VHP® LTS-V Low Temperature Sterilization - ISO 14937 Process  Validation Services | Al Bayan Health Care Solutions Co.Ltd
STERIS VHP® LTS-V Low Temperature Sterilization - ISO 14937 Process Validation Services | Al Bayan Health Care Solutions Co.Ltd

BS EN ISO 14937:2009
BS EN ISO 14937:2009

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 14937:2009 - 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 14937:2009 - Sterilization of health care products — General  requirements for characterization
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
BS EN ISO 14937:2009 Sterilization of health care products. General requirements for characterization of a

EN ISO 14937:2009 - Sterilization of health care products - General  requirements for
EN ISO 14937:2009 - Sterilization of health care products - General requirements for

SIST EN ISO 14937:2001 - Sterilization of health care products - General  requirements for
SIST EN ISO 14937:2001 - Sterilization of health care products - General requirements for

ASP Corporate PowerPoint Template
ASP Corporate PowerPoint Template

What is the level of treatment required for your endoscopes? - Steelco
What is the level of treatment required for your endoscopes? - Steelco

ISO 14937:2000, Sterilization of health care products - General  requirements for characterization of a sterilizing agent and the  development, ... a sterilization process for medical devices: ISO TC 198/WG  11: Amazon.com: Books
ISO 14937:2000, Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, ... a sterilization process for medical devices: ISO TC 198/WG 11: Amazon.com: Books

Sterilization Standards Update: Strategies for Compliance | PPT
Sterilization Standards Update: Strategies for Compliance | PPT

ANSI/AAMI/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
ANSI/AAMI/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 : 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 : 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

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
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