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PIB NO: 15.006 for ultrasound for vascular imagining for Israel

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PIB NO: 15.006 for ultrasound for vascular imagining for Israel


PIB NO:  15.006 for ultrasound for vascular imagining for Israel
DATE: 01/13/2015

Office of Acquisition Assistance Washington, D.C. 20523
Commodity Division (202) 569-4709


Item: Premium Ultrasound for Vascular Imaging    QTY: 1

Description : An advance Doppler with a peripheral vascular package and including independent pressure channels as well as PVR and PPG measurements.

Authority: AID Grant HSH-G-12-00032

Commodity ID no: Master list no B03

Date:  January 13 ,  2015                       

US Authorized Geographic code: 000                              

Country:              Israel


Purchasing agent

or Entity:            Hadassah Medical Organization

                          Kiryat Hadassah

                          P.O.B. 12000

                          IL-91120 Jerusalem, Israel

                         Fax: 011-972-2-6780821

Note: Hadassah Medical Organization requests bids for the commodities described above. To obtain a copy of the solicitation including the terms and specifications, please send a request to the Hadassah Medical Organization in Israel at

1. Fax no  972-2-6780821, clearly stating a fax number that can be reached 24 hours a day.

2. E-mail :

3. A copy can also be obtained from Mrs. Sandra Anasoulis at the Hadassah Medical Relief Association in New York,

tel: 212-303-8076 or fax no 212-303-8245. 

Please specify the equipment requested. Upon receipt of your request, a copy of the solicitation will be sent to you.

The deadline for submission of quotes is  Febr 28,  2015 4 p.m. local time

All manufacturers' warranties on proposed equipment must be honored in Israel.  The quotation must contain the name of a reliable Israeli agent that can carry out the terms of the warranty and who can be used for installation (if needed), spare parts and other services.

Offers are to be in compliance with USAID source, origin and nationality requirements enumerated in 22CFR, part 228.    

In order for a quote to be responsive to this notice, suppliers are required to provide a copy of the applicable approval letter from FDA, covering medical devices that require pre-market approval in the US.  

Additionally, the supplier shall provide the following certification :

“The undersigned supplier agrees and certifies that all products provided are covered by a valid FDA approval letter and/or otherwise are in compliance on the date of shipment with all applicable United States laws and regulations governing the delivery of regulated products in interstate commerce.”