Safety_IV_Catheters

The Defense Health Agency (DHA) Medical Logistics (MEDLOG) Division Medical Materiel Enterprise Standardization Office (MMESO) and the Defense Logistics Agency (DLA) Troop Support Medical Prime Vendor (PV) Program announce a Sources Sought Notification for the creation of a Qualified Suppliers Listing (QSL) for Safety IV Catheters. This is not a request for quote or proposal. The MMESO Pacific is the lead MMESO for this project. These Safety IV Catheters products are for purchase by the Military Treatment Facilities (MTFs) of the Military Health System (MHS) and for the operational assemblages of the Army, Navy, Air Force, Marine Corps, and Naval Expeditionary Medical Support Command (NEMSCOM) and managed regionally by MMESOs North, South, West, Pacific and Europe, hereafter referred to as MMESOs. For information regarding DLA Troop Support Medical's PV program please access its web site at https://www.medical.dla.mil. This Sources Sought notification is intended to solicit information and products for evaluation in order to create a QSL for Safety IV Catheters in accordance with (IAW) FAR 9.2. All items proposed to be included in this QSL must be on a Distribution and Pricing Agreement (DAPA) for the DLA Troop Support Medical/Surgical Prime Vendor (MSPV) Program. All participating vendors must complete the certification in the DAPA Management System (DMS). The MSPV Program requires that all items be manufactured in a Trade Agreements Act (TAA) Compliant Country (see DFARS 252.225-7020 AND 252.225-7021), unless it is determined that no functionally equivalent item is available from a compliant source. To be eligible for inclusion in the proposed QSL, all vendors are required to provide country of origin information in the QSL FBO Package Worksheet. In addition, according to the DAPA Terms and Conditions, you must complete the DAPA TAA Certification for each item offered. If an item offered is a TAA Non-Compliant End Product, the Government can use this information to determine whether or not a waiver exists or if the Government will seek a waiver for the item. Unless a waiver exists or is granted, TAA Non-Compliant County End Products cannot be added to the QSL and/or DAPA. Any questions concerning TAA may be directed to Donna Raday at DLA Troop Support, donna.raday@dla.mil, 215-737-7885. The QSL for Safety IV Catheters will be established approximately October 2016 and is anticipated to be the basis of a Standardization Action. Qualified vendors will be invited approximately November 2016 to submit pricing proposals to enter into an Incentive Agreement for Safety IV Catheters. The government reserves the right to standardize or not standardize on Safety IV Catheters. A. Products & Performance Required. The MMESOs are seeking product line items in the category of Safety IV Catheters. Within the MHS MTFs and operational procurement this product line has an estimated annual sales volume of $5,655,498.00. This forecast is based on historical usage data during a recent 12-month period. Twenty items are required for addition to the QSL and account for 76.5% ($4,328,352.00) of the total volume in sales ($5,655,498.00). The specifications for this project are shown in "Requirements to Qualify for QSL" section below. B. Instructions to Vendors Vendors interested in qualifying for inclusion in the QSL must provide an e-mail response to this QSL FBO Sources Sought notification to the lead MMESO POCs below. The vendor's responses must include all detailed information requested in the "Requirements to Qualify for QSL" section below and must also include: (1) Company name and address; (2) Company POC (Name and Phone Number, Fax Number, and E-mail address); (3) Commercial and Government Entity (CAGE) Code; and (4) Identification of the Sources Sought notification to which the vendor is responding. Due to the potential for e-mail to be lost in transmission, from network security, etc., vendors are strongly encouraged to confirm with the lead MMESO that their e-mail submission has arrived. Each submitting vendor is advised to confirm receipt, allowing adequate time for resubmission before the due date and time should a problem occur with the first submission. As part of the "Requirements to Qualify for QSL", vendors must complete and submit the QSL FBO Package Worksheet. Any vendor experiencing difficulty opening the Worksheet may contact the MMESO POCs. The MMESO POC will provide a Worksheet copy via an alternate method (fax, email or hard copy). Vendors that do not meet the deadline of COB 4:00 PM Hawaii Standard Time (HST) on the date listed for closing in this QSL FBO Sources Sought notification will not be included in the lead MMESO's review to establish the QSL and thus will not be able to participate in the subsequent Standardization Action. C. Source Selection Procedures The MMESO Joint Product Review Board (JPRB) will serve as the forum for clinical recommendations for product selection and coordinate logistics efforts in support of DoD Components. The board is chaired by Designated Senior Logisticians (DSLs) and co-chaired by Designated Senior Clinicians (DSCs) in the MMESO Areas of Responsibility (AORs) and includes clinicians and logisticians for MTFs within each MMESO. The Clinical Advisory Committee (CAC) members are the deciding officials for this initiative. The MMESO DSLs and DSCs intend to review responses and evaluate products for selection to the QSL IAW FAR 9.2. Requirements to Qualify for QSL The requirements for this product line are outlined below. Complete answers and all supporting documentation must be provided with the vendor's submittal by the response date stated in this QSL FBO Sources Sought notification. A vendor who does not meet all of these requirements or who does not submit documentation to support these requirements as requested will not be qualified for the QSL. Vendors must provide responses to this Sources Sought notification via the QSL FBO Package Worksheet. 1. Vendor must have a DAPA or be in the process of applying for a DAPA number for the product line listed. Vendor must provide their DAPA number or provide documentation and date the DAPA number was applied for. Vendors who do not continue to process application for a DAPA number will not be considered for continued participation. 2. Vendor must have an agreement with the current DoD Medical/Surgical Prime Vendor CARDINAL HEALTH, or must work with CARDINAL HEALTH to initiate an agreement. 3. Vendor must have an agreement with the current DoD Medical/Surgical Prime Vendor OWENS & MINOR, or must work with OWENS & MINOR to initiate an agreement. 4. Vendor must have a government issued Commercial and Government Entity (CAGE) code assigned for products contained within the specific product group or be in the process of obtaining one. Vendors must validate that their account is Active in the System for Award Management (SAM) and provide CAGE Code. Vendors in the process of obtaining a CAGE Code must provide documentation to support that they have registered in SAM. Vendors who do not continue to process application for a CAGE Code and/or a SAM account will not be considered for continued participation. See https://www.sam.gov/portal/public/SAM/. 5. Vendor offered products should be TAA compliant. End-items offered shall be manufactured or substantially transformed either in the U.S. or in Designated or Qualifying countries. Therefore, the vendor at the item level must provide country of origin for all required items and any optional items offered. Vendor must provide product catalog & literature for any items offered in response to this Sources Sought Notification. Vendor must submit the following information via QSL FBO Package Worksheet for each offered product: Full item description, Distributor Part Number, Manufacturer Part Number, Manufacturer Name, Number of eaches in Unit of Sale, and country of origin. Only ONE Vendor Part Number (PN) should be provided for each item/sample. Required Products / Annual Usage in Units / 1. 18 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 904,520 / 2. 20 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 394,050 / 3. 20 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 277,000 / 4. 20 GA 1 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 228,700 / 5. 16 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 151,190 / 6. 22 GA 1 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 153,420 / 7. 22 GA 1 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 138,900 / 8. 24 GA 3/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 83,750 / 9. 14 GA 1 3/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 44,400 / 10. 18 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 28,664 / 11. 18 GA 2 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 41,470 / 12. 20 GA 1 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 32,400 / 13. 20 GA 2 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 18,390 / 14. 18 GA 2 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 16,096 / 15. 14 GA 1 3/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 18,820 / 16. 14 GA 2 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 16,300 / 17. 24 GA 3/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 14,450 / 18. 16 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 11,550 / 19. 24 GA 1/2 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 4,700 / 20. 14 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 2,200 / 6. Vendor must provide Safety IV Catheter products that are not made with natural rubber latex and provide documentation to support this with initial submittal. 7. Vendor must provide Safety IV Catheter products that are sterile and provide documentation to support this with initial submittal. 8. Vendor must provide Safety IV Catheter products that are single-use and provide documentation to support this with initial submittal. 9. Vendor must provide Safety IV Catheter products that have the size, length and gauge marked on the packaging and provide documentation to support this with initial submittal. 10. Vendor must provide Safety IV Catheters with translucent plastic bodies and provide documentation to support this with initial submittal. 11. Vendor must provide Safety IV Catheter products that are radiopaque and provide documentation to support this with initial submittal. 12. Vendor must provide safety engineered Safety IV Catheter products and provide documentation to support this with initial submittal. 13. Vendor must provide manufacturer's instructions for use of Safety IV Catheter with this initial submittal. 14. Vendor must be able to provide in-service training as requested by the government. This in-service material requested may include the use of DVDs, in person training sessions; web based materials, or written materials (package inserts and literature). Vendor must provide documentation to support this with initial submittal. 15. Vendor must provide Safety IV Catheter with a sharps safety feature that can be activated using a single-handed gloved technique. 16. Vendor must provide Safety IV Catheter that allows the clinician's hand to remain behind the needle throughout the entire cannulation and sharps discard process. 17. Vendor must provide a Safety IV Catheter with a safety mechanism that will remain engaged throughout activation and the sharps disposal process. 18. Vendor may provide any or all of the additional items listed below, following the same format as for requirement number 5. Item Descriptions / 1. 18 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER WINGED / 2. 20 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER WINGED / 3. 14 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER WINGED / 4. 22 GA 1 INCH FEP RADIOPAQUE IV CATHETER WINGED / 5. 24 GA 5/8 INCH FEP RADIOPAQUE IV CATHETER WINGED / 6. 24 GA 1/2 INCH PUR RADIOPAQUE IV CATHETER WINGED / 7. 16 GA 2 INCH FEP RADIOPAQUE IV CATHETER WINGED / 8. 24 GA 1/2 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 9. 20 GA 1 INCH PUR RADIOPAQUE IV CATHETER WINGED / 10. 14 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 11. 16 GA 1 3/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 12. 14 GA 2 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 13. 16 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER WINGED / 14. 16 GA 1 3/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 15. 24 GA 3/4 INCH FEP RADIOPAQUE IV CATHETER WINGED / 16. 16 GA 2 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 17. 16 GA 2 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 18. 22 GA 3/4 INCH PUR RADIOPAQUE IV CATHETER WINGED / 19. 22 GA 1 3/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 20. 14 GA 2 INCH FEP RADIOPAQUE IV CATHETER WINGED / 21. 24 GA 5/8 INCH PUR RADIOPAQUE IV CATHETER WINGED / 22. 20 GA 1 3/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 23. 20 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER WINGED / 24. 24 GA 3/4 INCH PUR RADIOPAQUE IV CATHETER WINGED / 25. 18 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER WINGED / 26. 22 GA 1 INCH PUR RADIOPAQUE IV CATHETER WINGED / Evaluation After the lead MMESO receives all information required above, they will send each vendor making a complete and approved submission a written request to provide product samples to the Evaluation Site Leader (ESL) at the participating MTFs. MTF "Ship to" Addresses will be provided as part of the request. To ensure your eligibility to participate, all products required for evaluation must be shipped no later than 14 calendar days from issuance of the MMESO's request and must arrive at all designated MTFs no later than 5:00 PM local time at delivery location, 30 calendar days from issuance of the MMESO's request. Any products received after the stated date and time will not be included in review to establish the QSL and to participate in the subsequent Standardization Action, and will be destroyed upon receipt. Vendor will provide only the following products for evaluation. The products will be provided at no cost to the government for products or delivery, and unused products will not be returned. One (1) box of each gauge and length of the required items listed is to be provided as product samples to each of the evaluation sites as requested by the Lead MMESO. Vendor will be required to supply the same part number(s) submitted in the QSL FBO Package Worksheet. Items for Evaluation / 1. 18 GA 1 1/4 INCH PUR RADIOPAQUE IV CATHETER STRAIGHT / 2. 18 GA 1 1/4 INCH FEP RADIOPAQUE IV CATHETER STRAIGHT / 3. MANUFACTURER'S INSTRUCTIONS FOR SAFETY IV CANNULATION PROCESS / There will be approximately 25 MTFs enterprise wide that will be evaluating products. Each evaluator will evaluate the vendor submissions in the Safety IV Catheters product line. The MMESO Evaluation Site Leader will review the responses from the vendors and the results from the product evaluations and determine which vendors meet the requirements. A vendor who provides all requested information and meets the requirements will be selected for inclusion in the QSL. Vendors will be notified of whether they met or did not meet the QSL requirements by approximately November 2016. Points of Contact (POCs): Mr. Paul Davis, MMESO Pacific Team Leader, paul.j.davis.ctr@mail.mil, (808) 433-3686; and Ms. Maria Sheriff, RN, MMESO Pacific Clinical Analyst, maria.e.sheriff2.ctr@mail.mil, (808) 433-7985. DLA Troop Support Medical Contracting Officer: Tara J. Perrien, tara.perrien@dla.mil (215) 737-8307. The purpose of this Modification to the QSL FBO is to inform vendors on the QSL List that the Incentive Agreement FBO has now been posted. Only Vendors on the QSL for this product line can be considered for an IA. All solicitation information is available electronically on the Federal Business Opportunities website. Solicitation External Reference: https://www.fbo.gov/spg/DLA/J3/DSCP-M/IAP-1609-04/listing.html Solicitation External Reference To Packages: https://www.fbo.gov/spg/DLA/J3/DSCP-M/IAP-1609-04/packages.html