Tender detail

Centrifuge

Summary

The procurement concerns a centrifuge for a tissue bank. The bidder must supply a device that meets the technical specification and submit the required technical description, manufacturer information, representation-rights document, CE conformity documents and a cleanroom suitability document. The bid must also comply with the sanctions confirmation requirement.

Reference number
310467-0000
Buyer
Aktsiaselts Ida-Tallinna Keskhaigla
Country
Estonia (EST)
Procedure
Small procurement
CPV
33100000 Medical equipments
Deadline
2026-06-05
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 exclusion grounds include at least participation in a criminal organisation, corruption, fraud and other criminal-conviction grounds listed in the ESPD. The bidder must confirm whether any such grounds apply to the bidder or its management and representation persons within the last five years. If an exclusion ground exists, the bidder may submit evidence of self-cleaning measures where permitted. The machine-readable notice did not include precise exclusion grounds; they must be checked in the official tender documents.

Qualification criteria and exclusion grounds

The machine-readable notice did not include precise qualification, suitability or compliance requirements beyond the tender documents. The bidder must check the official tender documents for the exact requirements. The compliance conditions require the bid to match the technical specification, with Appendix 1 Technical Description completed and the manufacturer’s information material submitted. The bidder must be the official representative or reseller of the offered products in Estonia and submit the manufacturer’s confirmation of representation and sales rights. CE-marking compliance documents, including the EU declaration of conformity, must be submitted. A document confirming that the device is suitable for a cleanroom environment of at least class C must be submitted; the notice says that a technical datasheet, manufacturer confirmation or a risk analysis carried out by the bidder is sufficient evidence of GMP compliance. The bidder must also confirm that the bid is equivalent where relevant and that any equivalent solution is documented. The bidder must confirm that the offered goods are not subject to international sanctions and do not originate from sanctioned areas.