Tender detail

Glaucoma implants

Summary

The procurement concerns the purchase of glaucoma implants and the conclusion of a framework agreement for three years or until the maximum value is reached, whichever comes first. The procurement is divided into two lots, and tenders may be submitted for both lots, but a contract may be awarded to one bidder for a maximum of two lots. The bidder must prove the right to market the products in Estonia, the technical compliance of the products, CE marking and the availability of the required documents.

Reference number
312000-0000
Buyer
sihtasutus Tartu Ülikooli Kliinikum
Country
Estonia (EST)
Procedure
Open procedure
CPV
33190000 Miscellaneous medical devices and products
Deadline
2026-07-09
Status
Open
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 the mandatory exclusion grounds, including participation in a criminal organisation, corruption and other criminal-conviction-based 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; they must be checked in the tender documents.

Qualification criteria and exclusion grounds

The bidder must have the right to sell the offered products in Estonia. To prove this, the bidder must submit a document, or copy of a document, showing the manufacturer’s authorisation or, if the manufacturer is outside the European Union, the authorisation granted by the manufacturer’s authorised representative; in case of sub-delegation, the corresponding sub-delegation documents must also be provided. The offered products must comply with the technical descriptions in Annexes 1 and 2, and the bidder must submit the manufacturer’s detailed technical description, user manuals and other Estonian- or English-language materials proving compliance with the required characteristics. The offered products must bear the CE marking and be placed on the market in accordance with Regulation (EU) 2017/745 or its transitional provisions; copies of declarations of conformity and, where applicable, copies of certificates of conformity must be submitted, with the products offered in this procurement clearly highlighted. The bidder must submit the application for participation in the procurement according to Annex 4, Form II. In the case of a joint tender, a power of attorney for the joint bidders and a confirmation of joint and several liability must be submitted on Annex 4, Form I. The tender must comply with all conditions set out in the procurement documents, and conditional tenders are not allowed. The bidder must also confirm compliance with equivalence requirements where the offered solution relies on equivalence. The machine-readable notice did not include precise qualification or suitability criteria; they must be checked in the tender documents.