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FBO DAILY - FEDBIZOPPS ISSUE OF DECEMBER 08, 2017 FBO #5859
DOCUMENT

65 -- Snare Vascular Lead Extraction - Attachment

Notice Date

12/6/2017
 

Notice Type

Attachment
 

NAICS

#339112 — Surgical and Medical Instrument Manufacturing
 

Contracting Office

Department of Veterans Affairs;Network Contracting Office 20;960 Broadway Ave, Suite 460;Boise ID 83706
 

ZIP Code

83706
 

Solicitation Number

9187
 

Response Due

12/11/2017
 

Archive Date

12/31/2017
 

Point of Contact

Dan Salvesen
 

Small Business Set-Aside

N/A
 

Description

Sources Sought The purpose of this Sources Sought Announcement is for market research to make appropriate acquisition decisions and to gain knowledge of potential qualified Service Disabled Veteran Owned Small Businesses (SDVOSB), Veteran Owned Small Businesses (VOSB), 8(a), Hub-Zone and other Small Businesses interested and capable of providing items requested, as well as any large businesses The Department of Veterans Affairs, NCO20 is looking for sources of the following: QTY Item Model 2 EA SNARE, VASCULAR, LEAD EXTRACTION,13 MM LOOP, USABLE SHAFT LENGTH 94 CM, FEMORAL, NEEDLES EYE,DISPOSABLE,STERILE G26517 1 BX DEVICE, LEAD EXTRACTION, ONE-TIE COMPRESSION COIL G31929 5 EA LOCKING DEVICE, LEAD EXTRACTION, LEAD EXTENDER AID,FOR ALL COOK MEDICAL DILATOR SHEATH SETS, WORKING LENGTH 70 CM, STERILE G46542 1 BX DEVICE, LEAD EXTRACTOIN, GRIP-IT SHEATH GRIPPING PAD G52406 5 EA DEVICE, LEAD EXTRACTION, PIN VICE G20004 5 EA DEVICE, LEAD EXTRACTION, SOF-GRIP HEMOSTAT G20001 2 EA SET, LEAD EXTRACTION, EVOLUTION SHORTIE, RL ROTATING DILATOR,9FR G23748 2 EA SET, LEAD EXTRACTION,EVOLUTION SHORTIE, RL ROTATING DILATOR, 11FR G23749 The VAPORHCS Cath Lab is starting a Laser Lead Extraction Program. Spectranetics TightRail Mini, TightRail and TightRail Sub-C Rotating Dilator Sheaths are mechanical tools used for extraction of calcified pacemaker and defibrillator leads. Leads that have been implanted for years tend to develop calcification around their leads. The excimer laser (the normal removal method for lead extractions) does not work on calcified lesions. The TightRail provides a safe and efficient manual extraction method using a rotary cutter to remove these leads. Spectranetics SightRail Dilator Sheath Sets are mechanical tools used for the extraction of newly implanted (up to 12 months) pacemaker and defibrillator leads. The SightRail Dilator Sheath Set is a safe, efficient, cost effective alternative to the excimer laser (the normal removal method for lead extractions). Salient Characteristics for Manual Laser Lead Extraction Dilator Sheaths and Rotary Cutting Devices: Dilator Sheath Set for Manual Cardiac Pacemaker and ICD Lead Extractions: Dilator sheath set must be intended for use in patients requiring the percutaneous dilation of tissue to facilitate removal of cardiac leads. Dilator sheath set must be able to be used in conjunction with Spectranetics lead extraction tools (e.g., Spectranetics Lead Locking Stylets and Spectranetics VisiSheath Dilator Sheaths) Dilator sheath set must have printed indicators for bevel orientation and tip alignment. Dilator sheath sets must be visible using fluoroscopy. Dilator sheath sets must be available in 10 Fr. 11.5 Fr. and 13 Fr. sheath sizes. Dilator sheath set must be a telescoping system with an inner sheath and outer sheath. Inner sheath must be at least 43cm long. Outer sheath must be at least 33cm long. Telescoping system must have a least 10cm difference between inner and outer sheath to make the device easy to manipulate. 10Fr. Inner Sheath: Minimum Inner Diameter 9.6 Fr./0.127 in./3.2 mm Maximum Outer Diameter 12.5 Fr./0.163 in./4.2 mm 10 Fr. Outer Sheath: Minimum Inner Diameter 12.7 Fr./0.167 in./4.2 mm Maximum Outer Diameter 15.5 Fr./0.203 in./5.2 mm 11.5 Fr. Inner Sheath: Minimum Inner Diameter 11.2 Fr./0.147 in./3.7 mm Maximum Outer Diameter 14.0 Fr./0.183 in./4.7 mm 11.5 Fr. Outer Sheath: Minimum Inner Diameter 14.2 Fr./0.187 in./4.7 mm Maximum Outer Diameter 17.0 Fr./0.223 in./5.7 mm 13Fr. Inner Sheath: Minimum Inner Diameter 12.7Fr./0.167in./4.2mm Maximum Outer Diameter 15.5Fr./0.203in./5.2mm 13Fr. Outer Sheath: Minimum Inner Diameter 15.7Fr./0.207in./5.2mm Maximum Outer Diameter 18.6Fr./0.243in./6.2mm Dilator sheath set must be color coded (different color for each Fr. size sheath) Rotary Cutting Device for Manual Cardiac Pacemaker and ICD Lead Extraction: Rotating Dilator Sheath must be intended for use in patients requiring the percutaneous dilation of heavily fibrotic or calcific tissue to facilitate removal of cardiac leads. Rotating Dilator Sheath must be able to be used in conjunction with Spectranetics lead extraction tools (e.g., Spectranetics Lead Locking Stylets and Spectranetics VisiSheath Dilator Sheaths). Rotating Dilator Sheath must have a flexible shaft to help device remain coaxial to the lead. Rotating Dilator Sheath must be a handheld rotary cutter without the need for a power source with a dilating blade that remains shielded until activated. Rotating Dilator Sheath rotary cutter must have a bidirectional mechanism that is designed to effectively dilate commonly encountered fibrotic and calcific lesions. The bidirectional mechanism must be capable of rotating at least 574 degrees 287 degrees clockwise and 287 degrees counterclockwise. The bidirectional mechanism must not extend the cutting blade form than 0.5mm (0.02 inches) outside the shielded shaft. Rotating Dilator Sheath must have an optional static outer shaft that does not rotate with the blade (either included in the kit or sold separately) for use based on physician preference and the clinical scenario. Rotating Dilator Sheath must be available in at least two lengths Short (Working Length ~ 6.1 inches (15.5 cm) Long (Working Length ~ 18.7 inches (47.5cm) Rotating Dilator Sheath must be available in 9Fr., 11Fr. and 13 Fr. sheath sizes to accommodate different lead sizes and vessel diameters. Rotating Dilator Sheath product line must include a rotating dilator sheath designed specifically for treating fibrotic or calcific lesions in the subclavian vein. The intended contract is a firm-fixed price one-year contract. Potential contractors shall provide, at a minimum, the following information to daniel.salvesen@va.gov. 1) Company name, address, and point of contact, phone number, e-mail address, and DUNS. 2) Please identify your company s size in comparison to the anticipated North American Industry Classification System (NAICS) code 339112 Surgical and Medical Instrument Manufacturing. To be considered a small business your company must have fewer than 1,000 employees. This notice is to determine the marketplace for this specific requirement. Please check the following: [ ] yes [ ] no Service Disabled Veteran Owned Small Business (SDVOSB) [ ] yes [ ] no Veteran Owned Small Business (VOSB) [ ] yes [ ] no All other Small Business (SB) [ ] yes [ ] no Other than Small Business 3) The Government is not obligated to nor will it pay for or reimburse any costs associated with responding to this sources sought notice. This notice shall not be construed as a commitment by the Government to issue a solicitation or ultimately award a contract, nor does it restrict the Government to a particular acquisition approach. The Government will in no way be bound to this information if any solicitation is issued. Notice to Potential Offerors: All Offerors who provide goods or services to the United States Federal Government must be registered in the System Award Management (SAM located on the web at www.sam.gov). It is desirable that any Offeror to have completed their business Online Representations and Certifications Application in the System for Award Management (SAM). 4) Any Service Disabled Veteran Owned Businesses or Veteran Owned Businesses who respond to a solicitation on this project must be registered with the Department of Veterans Affairs Center for Veterans Enterprise VetBiz Registry located at http://vip.vetbiz.gov. 5) Only authorized representatives/providers of the manufacturer will be considered. Equipment must be new, no used or refurbished equipment accepted. Please provide a proof of authorized dealer or reseller letter from manufacturer. Responses are due by 12/11/2017 12:00 am EST, to the Point of Contact. Shipping Address: Boise VA Medical Center 960 Broadway STE 460 Boise, ID 83702 Point of Contact: Dan Salvesen Contracting Officer daniel.salvesen@va.gov 208-429-2021 ***** End Word Document - 'RFI-DESCRIPTION' ***** DISCLAIMER This RFI is issued solely for information and planning purposes only and does not constitute a solicitation. All information received in response to this RFI that is marked as proprietary will be handled accordingly. In accordance with FAR 15.201(e), responses to this notice are not offers and cannot be accepted by the Government to form a binding contract. Responders are solely responsible for all expenses associated with responding to this RFI.
 

Web Link

FBO.gov Permalink
(https://www.fbo.gov/spg/VA/BoVAMC531/BoVAMC531/9187/listing.html)
 

Document(s)

Attachment
 

File Name: 9187 9187_1.docx (https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=3948388&FileName=9187-000.docx)

Link: https://www.vendorportal.ecms.va.gov/FBODocumentServer/DocumentServer.aspx?DocumentId=3948388&FileName=9187-000.docx

 

Note: If links are broken, refer to Point of Contact above or contact the FBO Help Desk at 877-472-3779.
 

Place of Performance

Address: Department of Veterans Affairs;Portland VA Medical Center;3710 SW US Veterans Hospital Road;Portland OR

Zip Code: 97239
 

Record

SN04759052-W 20171208/171206231402-a31e507f669ee939391fc775634dd7e0 (fbodaily.com)
 

Source

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

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