SPECIAL NOTICE
65 -- Notice of Intent to Sole Source - NOI
- Notice Date
- 9/2/2016
- Notice Type
- Special Notice
- NAICS
- 339112
— Surgical and Medical Instrument Manufacturing
- Contracting Office
- Department of the Navy, Bureau of Medicine and Surgery, Naval Medical Logistics Command, 693 Neiman Street, FT Detrick, Maryland, 21702-9203, United States
- ZIP Code
- 21702-9203
- Solicitation Number
- N6264516RCES055
- Archive Date
- 10/1/2016
- Point of Contact
- Yun P. Hong, Phone: 3016194162
- E-Mail Address
-
yun.p.hong.civ@mail.mil
(yun.p.hong.civ@mail.mil)
- Small Business Set-Aside
- N/A
- Description
- NOI for 100NX DUO Upgrade Kit The Naval Medical Logistics Command (NMLC) intends to negotiate on a sole source basis (IAW FAR Part FAR 8.405-(6)(b)(1) Only one source is capable of responding). The proposed source is Johnson & Johnson Health Care Systems Inc. on behalf of Advanced Sterilization Products (JJHCS OBO ASP), 425 Hoes Lane, Piscataway, NJ 08854-4103. Naval Medical Center Portsmouth has a requirement for two (2) Sterilizing Units, Germicidal Gas, Gaseous Plasma and Naval Medical Center San Diego has a requirement for two (2) Sterilizing Units, Germicidal Gas, Gaseous Plasma. This requirement is part of Federal Supply Schedule (FSS) procurement. Only one award will be made as a result of this synopsis. The majority of the items required for the Sterilizing Units, Germicidal Gas, Gaseous Plasma are available on Federal Supply Schedule contract number V797P-4096B. However, the following component is not available via the FSS: 100NX DUO Upgrade Kit (PN: 10137). The system and all of the components, shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. The equipment and reagents shall be compliance with OSHA requirements. Vendor shall be an Original Equipment Manufacturer (OEM) authorized dealer, authorized distributor or authorized reseller for the proposed equipment/system such that OEM warranty and service are provided and maintained by the OEM. All software licensing, warranty and service associated with the equipment/system shall be in accordance with the OEM terms and conditions. Upon delivery, the vendor shall be responsible for uncrating the unit/system and transporting it through the facility to the location of intended use for installation, and removing of all trash created in this process. If interim storage is required, the vendor shall make arrangements for the storage. The system shall be compliant with the Food and Drug Administration (FDA) requirements to market and deliver medical products for use in the United States of America, even should delivery be requested outside of the United States. The claims made for the product shall comply with the regulations of the FDA with respect to products for marketing and delivery of a medical product for use in the United States of America, even should delivery be requested outside of the United States. The system shall be installed in compliance with OSHA requirements. If a vendor challenges the basis of this requirement, please email product capability statements (formats for submission: PDF, MS Word, or MS Excel) to Yun Hong at yun.p.hong.civ@mail.mil. Closing date for challenges is no later than 2:00 PM. Local Time on 16 Sep 2016. No phone calls will be accepted.
- Web Link
-
FBO.gov Permalink
(https://www.fbo.gov/spg/DON/BUMED/N62645/N6264516RCES055/listing.html)
- Record
- SN04254245-W 20160904/160902235245-eb970240bf927ce58776ea41aad387b5 (fbodaily.com)
- Source
-
FedBizOpps Link to This Notice
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