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Validation of instrument reprocessing methods for the Ipas manual vacuum aspiration devices

The objective of this study was to validate recommended reprocessing methods for Ipas manual vacuum aspiration (MVA) devices. The study found that Ipas MVA devices were not negatively affected following validated instrument reprocessing methods for high-level disinfection (HLD) or sterilization for up to 25 reuse cycles. STERRAD and Cidex OPA did not meet assessed standards and are therefore not recommended. Strict adherence to guidance is critical for effective reprocessing of instruments.

Authors: Bill Powell, Nathalie Kapp
Year: 2019

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We work with partners around the world to advance reproductive justice by expanding access to abortion and contraception.

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The global movement for legal, accessible abortion is growing. Our staff and partners in countries as diverse as Bolivia, Malawi and India are working to ensure all people can access high-quality abortion care.

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The global movement for legal, accessible abortion is growing. Our staff and partners in countries as diverse as Bolivia, Malawi and India are working to ensure all people can access high-quality abortion care.

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