Tender detail

Repeat procurement of CPAP accessories for the neonatology department – Lots 5 and 6

Summary

Aktsiaselts Ida-Tallinna Keskhaigla is procuring CPAP accessories for its neonatology department under a framework agreement, in two lots: a set of heated breathing-circuit tubing and water chamber for an active humidifier, and a T-piece resuscitation circuit for a resuscitation table.

Reference number
317281-0000
Buyer
Aktsiaselts Ida-Tallinna Keskhaigla
Country
Estonia (EST)
Procedure
Open procedure
CPV
33100000 Medical equipments
Deadline
2026-11-13
Status
Open
Contract subject
Supplies
Estimated value
Not published
Source
RHR

Participation requirements

Tender requirements are available in the official tender documents.

Compliance requirements

A bidder may be excluded for relevant final convictions involving participation in a criminal organisation, corruption, fraud, terrorist offences, money laundering or terrorist financing, child labour, or human trafficking, where the conviction concerns the bidder or a person in its management or with authority to represent or control it and was imposed within the previous five years or the exclusion period remains in force. Other grounds include unpaid taxes or social security contributions; insolvency, bankruptcy, liquidation, creditor arrangements, or suspended business; serious professional misconduct; agreements intended to distort competition; an unavoidable conflict of interest; involvement in preparing the procurement that creates an advantage that cannot otherwise be prevented; serious or repeated breaches of previous contracts resulting in early termination, damages, price reduction, or penalties; false or misleading information, failure to provide required information or documents, or attempts to obtain confidential information or improperly influence the decision. Grounds also include breaches of environmental, social, or labour-law obligations, enabling a person without lawful status to work, being subject to international sanctions, and conviction for tax offences. Where legally permitted, the bidder may provide evidence of measures taken to restore its reliability.

Qualification criteria and exclusion grounds

The supplied procurement documents do not specify financial-capacity, turnover, or experience thresholds. The bid must follow the technical description and be submitted using Annex 1, including the prescribed price structure. Bidders must provide manufacturer-issued product catalogues or other technical documentation demonstrating compliance. Products must carry CE marking, comply with Regulation (EU) 2017/745 on medical devices, and be DEHP-free; manufacturer-issued compliance documents are required for each product. If requested, original-packaged samples must be delivered within five working days of the request to Herne 29, Tallinn, with the procurement title, reference number, and bidder’s name marked on the sealed package. Failure to provide samples or a failed functional test may result in rejection. Any claimed equivalence must be explained and supported by evidence. Joint bidders must appoint an authorised representative and include their power of attorney. The bid must identify and justify any trade secrets; prices and other figures used for evaluation may not be classified as trade secrets. Bidders must confirm that the goods are not subject to international sanctions and are not from sanctioned regions. They must also confirm that they will not involve, for more than 10% of the contract value, subcontractors or suppliers who are Russian nationals, residents, or entities established in Russia, are more than 50% owned by such persons or entities, or act on their behalf or under their direction.