|SUPPLY AND DELIVERY OF CANNULA SPHINCTEROTOME WITH A TERM CONTRACT FOR 2 YEARS AND OPTION TO EXTEND FOR 2 YEARS|
The Sphincterotome is used during therapeutic endoscopic retrograde cholangio-pancreatogram (ERCP) procedures for cannulation and sphincterotomy.
In lieu of the current COVID-19, we will be accepting submission of RFP Documents and Annexes via email only during this period. Bidders are to adhere to the following instructions. We will not accept your submission if any Bidder did not adhere to the following:
- Submit your RFP proposal ONLY at 60mins before the RFP closing date & time (for e.g. Closing date: 29 October 2021, Closing time: 3pm. Bidder is to submit their proposal only on 29 October 2021, after 1400hrs, BUT not later than 1500).
2. In the email, Bidder must perform a print screen the
Pricing summary in Part 5 of your RFP document, in
order for us to correspond your submission to ensure
transparency in recording of price as of closing date
3. All submissions submitted after the closing time and
date, as of the PC time of receiving.
Bidder to submit his proposal in the form of TWO (2) softcopies (one editable softcopy and one scanned signed softcopy - by an authorised representative of bidder).
Publish Date (MM/DD/YYYY)
|10/15/2021 9:00 AM|
Closing Date (MM/DD/YYYY)
|10/29/2021 3:00 PM|
Extension Date (MM/DD/YYYY)
Tender Box No
|In lieu of the current COVID-19, we will be accepting submission of RFP Documents and Annexes via email only during this period.|
RFP/RFI/Tender documents are obtainable from the Buyer-in-charge via email: email@example.com
Please present the below in the email request.
(1) name of person in charge of this RFP/RFI/Tender
(2) valid EPPU / BCA registration (if applicable)
(3) non-refundable document fee (if applicable)
(4) duly signed Non-Disclosure Agreement (if applicable)
Site Showround / Briefing
Non-Disclosure Agreement (NDA)
Registration of Medical Devices from Health Science Authority (HSA)
Vendor shall ensure that the medical devices, with the exception of class A and B, delivered on or after 1 Aug 2010 to 31 December 2011 should either be:
a) registered on HSA Singapore Medical Device Register
b) placed on SMDR Transition List ; OR
c) cleared for import and supply through one of HSA Product
Registration special access routes
From 1 Jan 2012, all medical devices, class A, B, C, D, have to be registered with HSA SMDR.
The terms of this RFP/RFI/Tender have been posted at this site on the published date in their full intent and effect. CGH bears no responsibility for and shall not be bound by any changes made to such terms by unauthorised third parties. CGH does not guarantee that the terms received by you on this site comply with those as originally published. (If you wish to respond to this RFP/RFI/Tender, you are advised to verify such terms directly with CGH.) The Hospital does not bind itself to accept the lowest, the whole or any proposal.