Tender detail

Intravaskulaarse ja transuretraalse kehatemperatuuri kontrolli tarvikud

Summary

The tender concerns the purchase of intravascular and transurethral body temperature control accessories under a framework agreement. The procurement is divided into three lots, and a bid may be submitted for one or more lots. The bidder must also be prepared to provide product-use training at the contracting authority’s request, and the training must be delivered in Estonian. The bid must include technical descriptions, declarations of conformity, proof of representation rights and other required documents.

Reference number
309352-0000
Buyer
sihtasutus Tartu Ülikooli Kliinikum
Country
Estonia (EST)
Procedure
Open procedure
CPV
33141000 Disposable non-chemical medical consumables and haematological consumables
Deadline
2026-05-05
Status
Evaluation
Contract subject
Supplies
Estimated value
Not published
Source
RHR

Participation requirements

Tender requirements are available in the official tender documents.

Compliance requirements

The bidder must confirm that neither the company nor its management, administrative or supervisory body members, nor any person authorised to represent, decide for or control the company, has been finally convicted within the last five years for the listed exclusion grounds such as participation in a criminal organisation or corruption. If an exclusion ground applies, the bidder may have to show self-cleaning measures where allowed by law or the tender documents. The machine-readable notice did not include the full list of exclusion grounds, so the exact grounds and any required confirmations must be checked in the official tender documents.

Qualification criteria and exclusion grounds

The bidder must have sold each offered product, within the last 3 years before the contract notice was published, in a quantity of at least one third of the volume planned for the framework agreement period in Annex 1. To prove this, the bidder must submit a list of completed sales contracts or transactions showing the exact product name, quantity sold, contract dates, value and the other parties involved. The bidder must have a product representative working in the company or engaged on another contractual basis, and that person must have been trained by the manufacturer or completed training for the products covered by the tender. At the contracting authority’s request, copies of training certificates or a written confirmation from the manufacturer must be provided. The bid must comply with the technical descriptions in Annex 1. The bidder must submit the manufacturer’s detailed technical description, user instructions and other Estonian- or English-language materials showing compliance with the required characteristics. If the description contains company-specific terms, an explanatory document defining those terms must be added. The bidder must also provide proof of representation rights for the offered products if these were granted by the manufacturer or the manufacturer’s authorised representative. If someone other than the legal representative signs the bid, a power of attorney must be submitted. In the case of a joint bid, an authorised representative must be named and the joint bidders’ power of attorney and joint liability confirmation must be submitted. The bid must include the technical specification form from Annex 1, the forms from Annex 3, and a confirmation that the bid complies with the procurement documents and that the offered goods are not subject to international sanctions and do not originate from sanctioned regions. For CE-marked products, copies of the relevant certificates of conformity or declarations of conformity must be submitted. The machine-readable notice did not include all precise qualification details, so the official tender documents should be checked for any additional requirements or lot-specific conditions.