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Tristel Wipes Audit Checklist

by Curt Werner, from the Community

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Use this Tristel Wipes audit checklist to assess compliance with Standard 3.14 and infection control best practices for reprocessing non-lumen medical devices. Sections cover staff competency and recency, device identification and processing time, pre-clean wipe use, sporicidal wipe steps (activator foam pumps, 15-second scrunch, 30-second contact), traceability labeling, rinse wipe use, storage or patient-use documentation (labels, tracking book stamps, patient notes), final confirmation with printed name, date and signature, and optional microbiology testing within 3 months.

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Digitize any process, procedure or policy
Eliminate mistakes made by paper-based processes
Create and share professional reports instantly
Confirm accountability and compliance with a digital log

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This community page makes available free workplace checklists and templates created by other users within the SafetyCulture community. SafetyCulture has re-published this content and where possible, has credited the original author. SafetyCulture has not verified the accuracy, reliability or suitability of any community content. You agree that your use of any of this content is in accordance with SafetyCulture’s Terms and Conditions .