Tender detail

Immunoblot analyser and consumables

Summary

The tender concerns the purchase of an immunoblot analyser and consumables. The bidder must submit a compliant technical offer, proof from the manufacturer, proof of official representation and sales rights, a 4-year maintenance plan, and details of two trained medical technology specialists. The bidder must also confirm the exclusion grounds and sanctions-related declarations required by the tender documents.

Reference number
308606-0000
Buyer
Aktsiaselts Ida-Tallinna Keskhaigla
Country
Estonia (EST)
Procedure
Open procedure
CPV
33100000 Medical equipments
Deadline
2026-05-21
Status
Open
Contract subject
Supplies
Estimated value
479 000 EUR
Source
RHR

Participation requirements

Tender requirements are available in the official tender documents.

Compliance requirements

The bidder must confirm that neither it nor members of its management, administrative or supervisory bodies have been finally convicted within the last five years for participation in a criminal organisation, corruption, fraud, terrorism, money laundering, child labour, tax-related offences or other exclusion grounds listed in the tender documents. If an exclusion ground applies, the bidder may submit evidence of self-cleaning measures where permitted. The bidder must also confirm that it will not use subcontractors or suppliers linked to the Russian Federation for more than 10% of the contract value, and that the offered goods are not subject to international sanctions and do not originate from sanctioned areas.

Qualification criteria and exclusion grounds

The bidder must submit the technical specification and consumables form completed, and the bid must comply with the technical specification. Manufacturer information must be provided to prove that the offered device and accessories meet the requirements in the tender documents. The bidder must be the manufacturer’s official representative and must provide the manufacturer’s confirmation of representation and sales rights. The team must include two medical technology specialists who, from handover of the device until the end of the framework agreement, have received manufacturer training for maintenance and repair of the device; details of these specialists and the manufacturer’s training confirmation must be submitted. A compliant maintenance plan for 4 years of regular maintenance must also be submitted, showing the maintenance frequency, the work to be performed and the duration of one maintenance visit. The bid price must be submitted according to the required structure. If the bid is a joint bid, a power of attorney from the joint bidders must be attached. Conditional bids are not allowed.