Tender detail

Purchase of maintenance services and consumables for the LBC device 2

Summary

The procurement concerns a framework agreement for 4 years for maintenance of the Hologic ThinPrep 5000 Processor used to prepare liquid-based cytology (LBC) slides, and for the purchase of consumables needed for sample collection, transport and device operation. The bidder must meet registration, experience, technical capacity, representation rights, maintenance engineer and compliance requirements, and must submit the required declarations and supporting documents.

Reference number
313144-0000
Buyer
Sihtasutus Pärnu Haigla
Country
Estonia (EST)
Procedure
Open procedure
CPV
33141625 Diagnostic kits
Deadline
2026-08-27
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 that neither it nor the members of its management body have been finally convicted within the last five years for participation in a criminal organisation, corruption or fraud. If such a ground applies, evidence of self-cleaning measures must be provided where permitted. The notice also refers to other standard exclusion grounds, but the machine-readable text did not include the full list; the exact requirements must be checked in the tender documents.

Qualification criteria and exclusion grounds

The bidder must be registered in the commercial register or an equivalent register in its country of establishment, or submit a copy of the founding document if no registration obligation applies. The bidder must have completed at least 1 previous contract for consumables used with the Hologic ThinPrep 5000 Processor and maintenance services for that device. The total value of such contracts must be at least EUR 150,000. The bidder must submit a list of contracts completed during the 36 months before the start of the procurement, showing the contract value, dates and the other contracting parties. The bidder must have at least one licensed service engineer available both at the time of submitting the tender and throughout the contract period. The engineer must speak and write Estonian, and must have manufacturer training for servicing and repairing the offered device. The bidder must also provide the required declarations, proof of representation rights, product information, consumables lists, price list, maintenance plan, compliance confirmation and any documents proving conformity with EU in vitro diagnostic medical device requirements.