DOCUMENT
65 -- ENDOSCOPE REPROCESSING SYSTEM Medivators Advantage Plus - Attachment
- Notice Date
- 8/26/2016
- Notice Type
- Attachment
- NAICS
- 339113
— Surgical Appliance and Supplies Manufacturing
- Contracting Office
- Department of Veterans Affairs;Veterans Health Administration;Network Contracting Office 16;2575 Keystone Crossing;Fayetteville AR 72703
- ZIP Code
- 72703
- Solicitation Number
- VA25616Q1398
- Response Due
- 8/31/2016
- Archive Date
- 12/8/2016
- Point of Contact
- Dena Young
- Small Business Set-Aside
- Service-Disabled Veteran-Owned Small Business
- Description
- Department of Veterans Affairs Jack C. Montgomery VA Medical Center 1011 Honor Heights Dr Muskogee, OK 74401 The facility requires a minimum of three automatic endoscope reprocessors (AER) with a total capacity to reprocess 6 devices at one time. The AER must be validated for use with GI, Pulmonary, urology, and cardiac flexible scopes as well as ultrasound probes.The AER must be validated for use with GI, Pulmonary, urology, and cardiac flexible scopes as well as ultrasound probes. The facility is requesting three (3) FDA approved PA specific, high quality high-level disinfection system that is a fully automated, computer-based, asynchronous endoscope reprocessor. The reprocessor must have built in continuous leak testing and be able to detect a blockage in the scopes channel. The AER must be able to carry out a 70% isopropyl alcohol flush flowed by an air purge. Each AER must be able to run two scopes independently of each other in two separate compartments, with two separate sets of data for each scope's cycle. The AER's should have an average reprocessing time of 35 minutes which is inclusive of leak testing, washing, disinfecting, rinsing and final alcohol and air purge. The reprocessor must have a windows based software program that continuously monitors all parameters, system sensors and verification testing including but not limited to: control of machine draining, control of the pre-rinse and final rinse requirements and execution of the proper self-disinfection cycle, compromised endoscope sheath (leak detection), disconnected or improperly connected channels, channel blockage, reservoir temperatures, open chamber, deviation from maximum/minimum cycle step times, electrical power supply at incorrect cycle phase, disinfection contact times, inadequate and unsatisfactory completion of self-disinfection phase. Results must be recorded in the data management storage system for patient safety and quality assurance reporting. The reprocessor must have the ability for reprocessing soak-only devices. The AER must be compatible with the following endoscope hook-ups manufactured by Medivators: Bronchoscope Hook-up 2-8-210, Colonoscope hook-up 2-8-611 HAN, Gastrascope Hook-up 2-8-511 HAN, Cystoscope Hook-up 2-8-112, Transesophageal Echocardiogram Hook-up 2-8-001, Trans rectal Probe Hook-up 2-8-100 HAN, Pentax NasoPharyngoLaryngoscope Hook-up5-8-050 HAN.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/VA/FaVAMC564/FaVAMC564/VA25616Q1398/listing.html)
- Document(s)
- Attachment
- File Name: VA256-16-Q-1398 VA256-16-Q-1398_1.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=2971379&FileName=VA256-16-Q-1398-000.docx)
- Link: https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=2971379&FileName=VA256-16-Q-1398-000.docx
- Note: If links are broken, refer to Point of Contact above or contact the FBO Help Desk at 877-472-3779.
- File Name: VA256-16-Q-1398 VA256-16-Q-1398_1.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=2971379&FileName=VA256-16-Q-1398-000.docx)
- Record
- SN04242465-W 20160828/160826234351-d3f5ada6a278695cba3e27e8ba64ebdb (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
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