SOLICITATION NOTICE
65 -- Blood_Collection_Sets_Push_Button - QSL FBO Package Worksheet
- Notice Date
- 4/16/2014
- Notice Type
- Combined Synopsis/Solicitation
- NAICS
- 339113
— Surgical Appliance and Supplies Manufacturing
- Contracting Office
- Defense Logistics Agency, DLA Acquisition Locations, DLA Troop Support - Medical, 700 Robbins Avenue, Philadelphia, Pennsylvania, 19111-5096, United States
- ZIP Code
- 19111-5096
- Solicitation Number
- ME-1401-04
- Point of Contact
- Mr. Tom Winkel, Phone: 011-49-6371-9464-4089, Mr. Rob Halliday, Phone: 011-49-6371-9464-4090
- E-Mail Address
-
thomas.p.winkel.ctr@mail.mil, robert.b.halliday2.ctr@mail.mil
(thomas.p.winkel.ctr@mail.mil, robert.b.halliday2.ctr@mail.mil)
- Small Business Set-Aside
- N/A
- Description
- Complete answers and all supporting documentation must be provided with the vendor’s submittal by the response date stated in the 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. Vendor must provide responses to the Sources Sought notification via the QSL FBO Package Worksheet. 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 Blood Collection Sets Push Button. This is not a request for quote or proposal. The MMESO Europe is the lead MMESO for this project. These Blood Collection Sets Push Button 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, Europe, 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 in accordance with (IAW) FAR 9.2 for Blood Collection Sets Push Button. 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 (as defined by FAR 52.225-5), 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 complete the DAPA TAA Certification. Any questions concerning TAA may be directed to Bill Woltjen at DLA Troop Support, William.woltjen@dla.mil at 215-737-7124. The QSL for Blood Collection Sets Push Button will be established approximately September 2014 and is anticipated to be the basis of a Standardization Action. Qualified vendors will be invited approximately October 2014 to submit pricing proposals to enter into an Incentive Agreement for Blood Collection Sets Push Button. The government reserves the right to standardize or not standardize on Blood Collection Sets Push Button. A. Products & Performance Required. The MMESOs are seeking product line items in the category of Blood Collection Sets Push Button. Within the MHS MTFs and operational procurement this product line has an estimated annual sales volume of $1,885,334.17. This forecast is based on historical usage data during a recent 12-month period. The Blood Collection Sets Push Button represents nine distinct product groupings, of which nine are clinically significant. Five of those are requirements for addition to the QSL and accounts for $1,757,663.84 (93.23%) of the total volume in sales ($1,885,334.17). 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 5:00 PM Eastern Standard Time (EST) 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 instant 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 Blood Collection Sets Push Button requirements 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 who previously had an active record in Central Contractor Registration (CCR) 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 MUST provide the following items. 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, and Number of eaches in Unit of Sale. Only ONE Vendor Part Number (PN) should be provided for each item/sample. Required Products / Annual Usage in Units / Units of Sale (EACH) Safety blood collection set 23GA X 3/4 inch 12 inch tubing, push button, multi-sample, with threaded luer adapter, maximum unit of sale 200/each /781100 /200 Safety blood collection set 21GA X 3/4 inch 12 inch tubing, push button, multi-sample, with threaded luer adapter, maximum unit of sale 200/each / 507400 /200 Safety blood collection set 23GA X 3/4 inch 7-10 inch tubing, push button, multi-sample, with threaded luer adapter, maximum unit of sale 200/each / 36900 / 200 Safety blood collection set 21GA X 3/4 inch 7-10 inch tubing, push button, multi-sample, with threaded luer adapter, maximum unit of sale 200/each / 21700 / 200 Safety blood collection set 25GA X 3/4 inch 7-10 inch tubing, push button, multi-sample, with threaded luer adapter, maximum unit of sale 200/each / 4200 / 200 6. Vendor must provide safety push button blood collection sets that are sterile and documentation to support this with initial submittal. 7. Vendor must provide safety push button blood collection sets that are for single use and documentation to support this with initial submittal. 8. Vendor must provide safety push button blood collection sets that are Latex-free or Latex-safe and documentation to support this with initial submittal. 9. Vendor must provide safety push button blood collection sets that have a safety feature that cannot be deactivated and remains protective through disposal and documentation to support this with initial submittal. 10. Vendor must provide safety push button blood collection sets with a safety feature that is an integral part of the device and documentation to support this with initial submittal. 11. Vendor must provide safety push button blood collection sets with a safety feature that can be activated using a single-handed technique and documentation to support this with initial submittal. 12. Vendor must provide safety push button blood collection sets whose gauge size can be identified by color code and documentation to support this with initial submittal. 13. Vendor must provide safety push button blood collection sets that make an unmistakable change (audible or visible) when the safety feature is activated and documentation to support this with initial submittal. 14. Vendor must provide safety push button blood collection set with devices whose body and/or wings are ergonomically designed for improved handling and documentation to support this with initial submittal. 15. Vendor must provide sterile items with expiration dates printed on the unit of issue (i.e. box, individual package) and documentation to support this with initial submittal. 16. Vendor must provide safety push button blood collection sets with threaded luer adapters and documentation to support this with initial submittal. 17. Vendor must provide safety push button blood collection sets with translucent plastic bodies and documentation to support this with initial submittal. 18. Vendor must provide push button blood collection sets with the safety feature that does not impair the venipuncture process of inserting the needle into the vein. 19. Vendor must provide push button blood collection sets that allows the clinician's hands to remain behind the exposed sharp (needle point) during blood draw and safety feature activation. 20. Vendor must provide push button blood collection sets which connect securely to the tube holder and do not leak during the blood collection procedure. 21. Vendor MAY provide any or all of the optional items listed below, following the same format as for requirement number 5. Item Descriptions Safety blood collection set 25GA X 3/4 inch 12 inch tubing, multi-sample, with pre-attached holder Safety blood collection set 23GA X 3/4 inch 12 inch tubing with pre-attached holder Safety blood collection set 21GA X 3/4 inch 12 inch tubing, multi-sample, without luer adapter Safety blood collection set 21GA X 3/4 inch 12 inch tubing with pre-attached holder 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 Clinical Product Team (CPT) members 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 beyond the stated date and time will not be included in the CPT's reviews to establish the instant QSL and to participate in the subsequent Standardization Action, but 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 box of 48-50 each 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 Safety blood collection set 23GA X 3/4 inch 12 inch tubing, push button, multisample, with threaded luer adapter There will be approximately 14 MTFs enterprise wide that will be evaluating products. Each evaluator will evaluate the vendor submissions in the Blood Collection Sets Push Button product line. The MMESO CPT 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 September 2014. Points of Contact (POCs): Mr. Thomas Winkel, MMESO Europe Team Leader, thomas.p.winkel.ctr@mail.mil, (49) 6371-9464-4089; and Mr. Robert Halliday, MMESO Europe Clinical Analyst, robert.b.halliday2.ctr@mail.mil, (49) 6371-9464-4090. DLA Troop Support Medical Contracting Officer: Tara J. Perrien, tara.perrien@dla.mil (215) 737-8307.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/DLA/J3/DSCP-M/ME-1401-04/listing.html)
- Place of Performance
- Address: ERMC HQ, CMR 402 box 219, Dept G4, Bldg 3739, Rm 222, Landstuhl, Rhineland-Palatinate, Non-U.S., APO 09180-, United States
- Record
- SN03339979-W 20140418/140416234609-2cb2a3c792ef5e14e84ef1eb9cd010af (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
(may not be valid after Archive Date)
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