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FBO DAILY - FEDBIZOPPS ISSUE OF SEPTEMBER 11, 2016 FBO #5406
MODIFICATION

65 -- Exam_Gloves

Notice Date

9/9/2016
 

Notice Type

Modification/Amendment
 

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

MW-1510-57
 

Point of Contact

Mr. Ricardo U. Orias, Phone: (619) 532-8537, Mr Redentor Sese, Phone: (619) 532-8517
 

E-Mail Address

ricardo.u.orias.ctr@mail.mil, redentor.p.sese.ctr@mail.mil
(ricardo.u.orias.ctr@mail.mil, redentor.p.sese.ctr@mail.mil)
 

Small Business Set-Aside

N/A
 

Description

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 Exam Gloves. This is not a request for quote or proposal. The MMESO West is the lead MMESO for this project. These Exam Gloves 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 Exam Gloves 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). 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. Offers of U.S. made, qualifying country, or designated country end products from responsive, responsible offerors are currently not available for the procurement of Exam Gloves. DLA has been granted an exception for synthetic medical exam gloves manufactured in Malaysia or Thailand. As a result of that exception, this sources sought notification is being modified to allow submissions of TAA non-compliant synthetic medical exam gloves manufactured in Malaysia or Thailand. Any questions concerning TAA may be directed to Donna Raday at DLA Troop Support, donna.raday@dla.mil, 215-737-7885. The QSL for Exam Gloves will be established approximately February 2017 and is anticipated to be the basis of a Standardization Action. Qualified vendors will be invited approximately March 2017 to submit pricing proposals to enter into an Incentive Agreement for Exam Gloves. The government reserves the right to standardize or not standardize on Exam Gloves. A. Products & Performance Required. The MMESOs are seeking product line items in the category of Exam Gloves. Within the MHS MTFs and operational procurement this product line has an estimated annual sales volume of $12,639,253.00. This forecast is based on historical usage data during a recent 12-month period. There are five (5) required Exam Glove items the vendor must provide for addition to the QSL. These required items account for 89.28% ($11,284,988.00) of the total volume in sales ($12,639,253.00). 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 email 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 email 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, e-mail or hard copy). Vendors that do not meet the deadline of COB 5:00 PM Pacific Standard Time (PST) 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. Offers of U.S. made, qualifying country, or designated country end products from responsive, responsible offerors are currently not available for the procurement of Exam Gloves. DLA has been granted an exception for synthetic medical exam gloves manufactured in Malaysia or Thailand. As a result of that exception, this sources sought notification is being modified to allow submissions of TAA non-compliant synthetic medical exam gloves manufactured in Malaysia or Thailand. 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, 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 / 5.1 EXAM GLOVES, NITRILE NS PF LG / 52,831,770 / 5.2 EXAM GLOVES, NITRILE NS PF MED / 75,090,350 / 5.3 EXAM GLOVES, NITRILE NS PF SM / 43,891,100 / 5.4 EXAM GLOVES, NITRILE NS PF XL / 11,244,130 / 5.5 EXAM GLOVES, NITRILE NS PF XS / 1,628,600 / 6. Vendor must provide Exam Gloves that are FDA approved and provide documentation to support this with initial submittal. 7. Vendor must provide Exam Gloves that meet the ASTM D6319 (Standard Specification for Nitrile Examination Gloves for Medical Application) and provide documentation to support this with initial submittal. 8. Vendor must provide Exam Gloves products that are not made with natural rubber latex and provide documentation to support this with initial submittal. 9. Vendor must provide Exam Gloves products that are powder-free (PF) and provide documentation to support this with initial submittal. 10. Vendor must provide Exam Gloves with box packaging that indicates single use and provide documentation to support this with initial submittal. 11. Vendor must provide Nitrile Exam Gloves products with length of at least 9 inches and no more than 10 inches and provide documentation to support this with initial submittal. 12. Vendors much provide Nitrile Exam Gloves products with 2.8 mil to 6 mil finger thickness and provide documentation to support this with initial submittal. 13. Vendor must provide Nitrile Exam Gloves products in blue, lavender, purple, or gray color and provide documentation to support this with initial submittal. 14. Vendor must provide Exam Gloves products that are ambidextrous, with a beaded cuff, and textured finger tips and provide documentation to support this with initial submittal. 15. Vendor must provide Exam Gloves with box packaging that includes product size, type, and latex content and provide documentation to support this with initial submittal. 16. Vendor must provide products that are intact and without any evidence of tearing or holes before donning, during donning, while performing hand movements, and after removal of gloves. 17. Vendor must provide Exam Gloves that do not elicit signs of skin irritation (drying, itching, redness, urticaria) after five minutes of wearing. Vendor may provide any or all of the optional items listed below, following the same format as for requirement number 5. Item Descriptions / 1. EXAM GLOVES, NITRILE NS PF LG BLACK / 2. EXAM GLOVES, NITRILE NS PF LG EXT CUFF / 3. EXAM GLOVES, NITRILE NS PF LG EXT CUFF WITH ALOE / 4. EXAM GLOVES, NITRILE NS PF LG WITH ALOE / 5. EXAM GLOVES, NITRILE NS PF MED BLACK / 6. EXAM GLOVES, NITRILE NS PF MED EXT CUFF / 7. EXAM GLOVES, NITRILE NS PF MED EXT CUFF WITH ALOE / 8. EXAM GLOVES, NITRILE NS PF MED WITH ALOE / 9. EXAM GLOVES, NITRILE NS PF SM BLACK / 10. EXAM GLOVES, NITRILE NS PF SM EXT CUFF / 11. EXAM GLOVES, NITRILE NS PF SM WITH ALOE / 12. EXAM GLOVES, NITRILE NS PF XL BLACK / 13. EXAM GLOVES, NITRILE NS PF XL EXT CUFF / 14. EXAM GLOVES, NITRILE NS PF XL WITH ALOE / 15. EXAM GLOVES, NITRILE NS PF XS BLACK / 16. EXAM GLOVES, NITRILE NS PF XS EXT CUFF / 17. EXAM GLOVES, NITRILE NS PF XS WITH ALOE / 18. EXAM GLOVES, NITRILE NS PF XXL / 19. EXAM GLOVES, NITRILE NS PF XXL EXT CUFF / 20. EXAM GLOVES, NITRILE STERILE PF LG / 21. EXAM GLOVES, NITRILE STERILE PF MED / 22. EXAM GLOVES, NITRILE STERILE PF SM / 23. EXAM GLOVES, NITRILE STERILE PF XL / 24. EXAM GLOVES, SYNTHETIC CHLOROPRENE NS PF LG / 25. EXAM GLOVES, SYNTHETIC CHLOROPRENE NS PF MED / 26. EXAM GLOVES, SYNTHETIC CHLOROPRENE NS PF SM / 27. EXAM GLOVES, SYNTHETIC, CHLOROPRENE NS PF XL / 28. EXAM GLOVES, SYNTHETIC, CHLOROPRENE NS PF XS / 29. EXAM GLOVES, VINYL NS PF LG / 30. EXAM GLOVES, VINYL NS PF MED / 31. EXAM GLOVES, VINYL NS PF SM / 32. EXAM GLOVES, VINYL NS PF XL / 33. EXAM GLOVES, VINYL NS PF XS / 34. EXAM GLOVES, VINYL STERILE PF LG / 35. EXAM GLOVES, VINYL STERILE PF MED / 36. EXAM GLOVES, VINYL STERILE PF SM / 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 box of at least 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 / EXAM GLOVES, NITRILE NS PF MED / EXAM GLOVES, NITRILE NS PF LG / There will be approximately 7 MTFs enterprise-wide that will be evaluating products. Each evaluator will evaluate the vendor submissions in the Exam Gloves 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 February 2017. Points of Contact (POCs): Mr. Ricardo Orias, MMESO West Team Leader, ricardo.u.orias.ctr@mail.mil, 619-532-8537; and Mr. Redentor Sese, RN, MMESO West Clinical Analyst, redentor.p.sese.ctr@mail.mil, 619-532-8517. 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/MW-1510-57/listing.html)
 

Place of Performance

Address: Medical Materiel Enterprise Standardization Office (MMESO) West, 34960 Bob Wilson Dr., San Diego, California, 92134, United States

Zip Code: 92134
 

Record

SN04265346-W 20160911/160911093002-3508ef975ead24869a0ddbebd9e5a640 (fbodaily.com)
 

Source

FedBizOpps Link to This Notice
(may not be valid after Archive Date)

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