Ethylene Oxide EO Sterilization Validation Procedure | ISO 13485 | FDA QSR Compliant
SKU:
SOP 7-035
$149.00
$149.00
per item
The Ethylene Oxide (EO) Sterilization Validation Procedure governs the requirements for the validation, revalidation, adoption, and routine sterilization of medical devices by EO gas in accordance with ISO 11135.
- ISO 11135 Compliant
- ISO 10993-7 Compliant
- ISO 13485 Compliant
- FDA QSR Compliant
- MS Word Format
- Digital Content - Instant Download
EO Sterilization Validation ProcedureThe ISO 13485 Ethylene Oxide (EO) Sterilization Validation Procedure defines the planning and testing requirements for conducting the validation, re-validation, adoption and routine sterilization of medical devices by ethylene oxide (EO) gas in accordance with ISO 11135.
EO Sterilization Validation Procedure OverviewThe EO Sterilization Validation Procedure includes guidance on development of EO validation protocols including test considerations, selection of master challenge device, identification and placement of biological indicators (BI's) and more,
The procedure includes guidance on routine monitoring and instruction on how to evaluate products for adoption into an existing EO sterilization cycle. along with required documentation. The EO Sterilization Validation Procedure also provides guidance on how to group products EO sterilization product families and the establishment of an EO processing category. EO Sterilization Validation Procedure ComplianceThe Ethylene Oxide (EO) Sterilization Validation Procedure is ISO 11135 ISO 10993-7, FDA QSR and ISO 13485 compliant.
To learn more about our Ethylene Oxide (EO) Sterilization Validation Procedure contact us at [email protected]
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