Tender detail

Hydrocephalus treatment devices

Summary

The tender concerns sterile single-use medical devices for the treatment of hydrocephalus: fixed-pressure and adjustable valves, catheters and external drainage devices. Bids are to be submitted by lot, up to 4 lots, and a contract may also be awarded to one bidder for up to 4 lots. The bid must comply with the tender documents and include the required forms, technical information, a document proving the manufacturer’s or authorised supplier’s sales/technical support rights, and, for medical devices, the instructions for use, the declaration of conformity and, where applicable, the EC certificate.

Reference number
305464-0000
Buyer
sihtasutus Põhja-Eesti Regionaalhaigla
Country
Estonia (EST)
Procedure
Open procedure
CPV
33141000 Disposable non-chemical medical consumables and haematological consumables
Deadline
2026-05-29
Status
Open
Contract subject
Supplies
Estimated value
409 000 EUR
Source
RHR

Participation requirements

Tender requirements are available in the official tender documents.

Compliance requirements

The tender documents include the standard exclusion grounds from the Public Procurement Act, especially convictions for participation in a criminal organisation, corruption, fraud and other mandatory exclusion grounds. The bidder must confirm the exclusion questions and, where applicable, provide details of convictions, self-cleaning measures and electronic evidence. The machine-readable notice did not include the full list of exclusion grounds; they must be checked in the official tender documents.

Qualification criteria and exclusion grounds

The bidder must meet the qualification and compliance requirements set out in the ESPD and the tender documents. The machine-readable notice did not include precise qualification requirements; they must be checked in the official tender documents. According to the compliance requirements, the bidder must confirm that the bid complies with all tender document requirements, submit the completed participation application, the completed technical specification and the price form, and attach technical information. The bidder must also provide a document proving the manufacturer’s or authorised supplier’s right to represent the offered products, the package labelling, and, for medical devices, the instructions for use, the manufacturer’s declaration of conformity and, where applicable, the EC certificate. If an equivalent product is offered, equivalence must be explained and supported by evidence. In addition, the bidder must confirm that it will not use subcontractors or suppliers linked to the Russian Federation sanctions regime 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. In the case of a joint bid, a power of attorney for the joint bidders must be attached. If the bidder wants to rely on a climate and environmental impact reduction goal, that goal must be publicly available and meet the conditions described in the tender documents. The machine-readable notice did not include precise qualification requirements; they must be checked in the official tender documents and tender documents.