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PIB NO: 15.059 For a cardiological ultrasound machine to Israel

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PIB NO: 15.059 For a cardiological ultrasound machine to Israel

PIB NO: 15.059 For a cardiological ultrasound machine to Israel
DATE: 9/21/2015
Office of Acquisition Assistance Washington, D.C. 20523
Commodity Division

Item: Cardiological Ultrasound QTY: 1
Description: This cardiological Ultrasound machine is to be used for all exams performed on a diverse population starting with including neonates, children, adolescents and going up to adults. For this we require a machine with imaging modes from 2D to 4D, color Doppler and live real time imaging
Authority: AID Grant HSH-G-13-00024
Commodity ID no: Master list no A04

Date: September 21 , 2015

US Authorized Geographic code: 937
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 Nov. 5, 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.”