Scope reprocessor test

    • [DOCX File]www.vendorportal.ecms.va.gov

      https://info.5y1.org/scope-reprocessor-test_1_ebbaa7.html

      SCOPE OF WORK. For. STERILIZER, REPROCESSOR, WASHER, AND GUS VAPOR CONTROL . SERVICE. ... replace parts, test for operating efficiency and other such items in accordance with the terms, conditions, provisions and specifications contained herein, and in accordance with manufacturer’s instructions and specifications, herein, called service. The ...

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    • [DOC File]Report - APIC

      https://info.5y1.org/scope-reprocessor-test_1_b3a1f8.html

      Immediately after the procedure, wipe off the scope with a damp cloth or 4x4 to remove any gross debris, then wrap in a clean towel and take to the soiled utility room. Always wear gloves to handle a dirty scope. Wear gown and face protection if splashing is likely. Perform the leak test by connecting the scope to the leak test device. REQUIRED!

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    • [DOC File]Restraint Competency Verification - APIC

      https://info.5y1.org/scope-reprocessor-test_1_8b03a1.html

      Automated Endoscope Reprocessor (AER) High-Level Disinfection 1. Test the potency of the disinfectant solution according to the manufacturer’s instructions 2. Inspect the connections according the AER manufacture’s instructions 3.

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    • [DOCX File]Beth Israel Deaconess Medical Center

      https://info.5y1.org/scope-reprocessor-test_1_2a1b08.html

      Probe Reprocessor with. OPA. Check that all system fluid levels are adequate. Equipment specifics: Wipe system with PDI AF-3 Sani Wipes. Insert the probe into the TEE probe block opening, insuring that the immersible probe parts are inserted completely up to the handle. Support the handle on rack above.

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    • [DOCX File]APIC MT

      https://info.5y1.org/scope-reprocessor-test_1_216248.html

      Circle manual clean/disinfection or automated reprocessor (AR) used, list brand. Y N. ... Manual leak test: Staff know what to do if continuous stream of bubbles seen on leak test. Y. N. ... Tag with date on scope(s) hanging in storage cabinet. Infrequently used scope reprocessed with facility hang time prior to a scheduled procedure. Y. N.

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    • [DOCX File]Oregon Patient Safety Commission | Advancing Patient ...

      https://info.5y1.org/scope-reprocessor-test_1_65749a.html

      Procedures to validate and record the testing of the chemical concentration test strips and the labeling of the expiration date on the test strip vials. All PPE (e.g., gloves, gowns, eyewear, face mask or shields, respiratory protection devices) should be readily available to personnel performing endoscope reprocessing procedures

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    • [DOCX File]Sample Gap Analysis Tool: Reprocessing Flexible Endoscopes

      https://info.5y1.org/scope-reprocessor-test_1_8e04c1.html

      A gap analysis is a way for facilities to determine if facility endoscope reprocessing practices are aligned with best practices and manufacturer’s IFU and to determine if a plan of action should be created to move from current practices to implementation of best practices for scope processing.

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    • [DOCX File]www.vendorportal.ecms.va.gov

      https://info.5y1.org/scope-reprocessor-test_1_5f7a43.html

      March 2010JFY17 OER-Pro Endoscope Reprocessor Service19805VA244-17-Q-006810-25-20163811219Department of Veterans AffairsNetwork Contracting Office 4April StanchApril.Stanch@va.govLebanon VA Medical Center1700 South Lincoln AveLebanon17042USA ... Scope of Work: In accordance with the following specifications: ... tools, test equipment, service ...

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    • [DOC File]Easi-Sterilise Audt Tool: Operations

      https://info.5y1.org/scope-reprocessor-test_1_654c31.html

      ( Leak test is performed as per manufacturer’s instructions ( Manufacturer’s cleaning instructions are available and followed ( Appropriate enzymatic detergents/biofilm removal agents are used ( Warm water (35 C) is used with enzymatic solution for optimum efficacy ( Detergent and water dilution is measured to ensure correct dilution ...

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    • CHAPTER I: SCOPE AND DEFINITIONS

      The reprocessor of the device shall be considered to be a producer for the purpose of Article 3(1) of Directive 85/374/EEC. By way of derogation from paragraph 2, as regards single-use devices that are reprocessed and used within a health institution, Member States may decide not to apply all of the rules relating to manufacturers' obligations ...

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