Retender: International Competitive Bidding - Request for Quotation (RFQ): Supply of medical devices to the Lagos State Ministry of Health of Nigeria

New amendment added #1: The purpose of this amendment is to extend the submission deadline from October 17, 2025 22:59 UTC to October 24, 2025 22:59 UTC

New clarification added: Dear UNOPS, Will you please extend the dealine of this tender, as we are facing challenges to obtain quotes. Kind RegardsAnswer:The deadline for this tender will be extended through a tender amendment that will be posted on eSourcing.

New clarification added: Dear Sir or Madam,In order to supply correct product and service, please allow me to ask the following question: About the following item, it is must be satisfied?1.2 /2.4 Mandatory: Must have a valid  NAFDAC registration in Nigeria. Provide the valid product registration certificate or NAFDAC Import permit. This is a prerequisite to importation into Nigeria1.3/2.5  Mandatory: The product shall have medical device regulatory approval or marketing authorisation issued by the EU (CE) or US (FDA), or other GHTF founding members such as Australia, Canada or Japan or be prequalified by WHO Products without this certification will be disqualified.Your early reply would be appreciated!ANSWERUNOPS will accept all detailed technical specifications for products that meet the following mandatory requirements;Must have a valid NAFDAC registration in Nigeria. Provide the valid NAFDAC product registration certificate or NAFDAC Import permit. Products without this cannot be imported into Nigeria.The product shall have medical device regulatory approval or marketing authorisation issued by the EU (CE) or US (FDA), or  other GHTF founding members such as Australia, Canada or Japan or be prequalified by WHO. Products without this will be disqualifiedThe product is manufactured under a certified Quality Management System (QMS). Provide the Manufacturer's ISO 13485 or ISO 9001 certified QMS, issued by a Notified Body or a body accredited by the IAF (International Accreditation Forum). Products without this will be disqualifiedTks&RgsFeng Li

New clarification added: Dear Sir/ MadamGood day!For IV giving set or infusion set, could you share me the picture of the product you need, if possible with specification like tube length, package materialyour positive and quick response will highly be appreciatedAnswer: UNOPS will accept all detailed technical specifications for products that meet the following mandatory requirements or else the product will be disqualified;Must have a valid NAFDAC registration in Nigeria. Provide the valid NAFDAC product registration certificate or NAFDAC Import permit. Products without this cannot be imported into Nigeria.The product shall have medical device regulatory approval or marketing authorisation issued by the EU (CE) or US (FDA), or  other GHTF founding members such as Australia, Canada or Japan or be prequalified by WHOThe product is manufactured under a certified Quality Management System (QMS). Provide the Manufacturer's ISO 13485 or ISO 9001 certified QMS, issued by a Notified Body or a body accredited by the IAF (International Accreditation Forum).

New clarification added: Dear Sir/MadamWe feel this tender is missing specifications and descriptions, That is to say,1. For infusion giving set, there are so many different models with different configuration, this tender just gave simple product name without any details.2. For IV cannulas, there are pen like & with wing & with wing and injection port & safety different models, which model do they need?your quick response will highly be appreciatedANSWERUNOPS will accept all detailed technical specifications for products that meet the following mandatory requirements or else the product will be disqualified;Must have a valid NAFDAC registration in Nigeria. Provide the valid NAFDAC product registration certificate or NAFDAC Import permit. Products without this cannot be imported into Nigeria.The product shall have medical device regulatory approval or marketing authorisation issued by the EU (CE) or US (FDA), or  other GHTF founding members such as Australia, Canada or Japan or be prequalified by WHOThe product is manufactured under a certified Quality Management System (QMS). Provide the Manufacturer's ISO 13485 or ISO 9001 certified QMS, issued by a Notified Body or a body accredited by the IAF (International Accreditation Forum).