Tender detail

Allergy and autoimmune test reagents with equipment use

Summary

The tender concerns the purchase of allergy and autoimmune test reagents together with the free use of the equipment needed to use them. The tender is divided into two lots, and bids may be submitted for both lots, but a contract may be awarded to one bidder for a maximum of two lots. The bidder must confirm compliance with the tender documents and submit the required contact details, technical description, manufacturer documentation, instructions for use, and proof of the medical technology specialists and representation rights.

Reference number
312923-0000
Buyer
Aktsiaselts Ida-Tallinna Keskhaigla
Country
Estonia (EST)
Procedure
Open procedure
CPV
33190000 Miscellaneous medical devices and products
Deadline
2026-08-17
Status
Open
Contract subject
Supplies
Estimated value
1 632 000,00 EUR
Source
RHR

Participation requirements

Tender requirements are available in the official tender documents.

Compliance requirements

The bidder must confirm the standard exclusion grounds in the ESPD/hankepass, including criminal organisation, corruption and other mandatory grounds set out in the tender documents. If an exclusion ground applies, the bidder may provide evidence of self-cleaning where allowed. The machine-readable notice did not include the full list of exclusion grounds in the excerpt provided, so the exact grounds must be checked in the official tender documents.

Qualification criteria and exclusion grounds

The bidder must submit the required technical and compliance documents: the technical description form, product documentation proving conformity, instructions for use, an Estonian user manual, an English user manual, and the LIS interface communication specification if applicable. The bidder must also provide the contact details of the person signing the framework and contract documents and the contact person for contract performance, a power of attorney for joint bidders if applicable, and a maintenance plan covering 4 years of regular maintenance. The team must include 2 medical technology specialists trained by the manufacturer for servicing and repairing the offered device, and their work language must be Estonian. The bidder must be the manufacturer’s official representative and provide proof of representation and sales rights. The notice also requires confirmation that the bid is unconditional, that the bid price form structure is followed, and that the offered goods are not subject to international sanctions and are not supplied through prohibited Russian-related subcontractors or suppliers. The machine-readable notice did not include all precise qualification and compliance requirements in the excerpt provided, so the official tender documents must be checked for any additional details.