Tender detail

Purchase of physiotherapy equipment and patient training equipment

Summary

The tender concerns the purchase of physiotherapy equipment and patient training equipment. Lot 1 and Lot 2 include at least 7 years of post-warranty maintenance, repairs and spare parts; Lot 3 includes 4 years. A bid may be submitted for all lots, but a single bidder may be awarded up to 3 lots. The required forms, technical documentation, user manual and confirmations of product compliance and sanctions-related requirements must also be submitted.

Reference number
310367-0000
Buyer
Aktsiaselts Lääne-Tallinna Keskhaigla
Country
Estonia (EST)
Procedure
Open procedure
CPV
33155000 Physical therapy devices
Deadline
2026-06-25
Status
Evaluation
Contract subject
Supplies
Estimated value
28 750,00 EUR
Source
RHR

Participation requirements

Tender requirements are available in the official tender documents.

Compliance requirements

The bidder must confirm that neither the bidder nor its management bodies have been finally convicted within the last five years for participation in a criminal organisation, corruption, fraud and other exclusion grounds listed in the ESPD, or that any exclusion period has expired. If an exclusion ground applies, the bidder may submit evidence of self-cleaning measures where permitted. The bidder must also confirm that the offered goods are not subject to international sanctions and do not originate from sanctioned areas, and that subcontractors or suppliers subject to sanctions will not account for more than 10% of the contract value.

Qualification criteria and exclusion grounds

The machine-readable notice did not include precise qualification or suitability criteria; these must be checked in the official tender documents. The ESPD and compliance documents nevertheless require the bidder to submit the mandatory forms 1, 2 and 3 for the relevant lot, manufacturer and supplier warranty terms, spare parts warranty terms, maintenance requirements and recommendations, the technical description and manufacturer documentation, and the user manual. The offered device must be proven to be a medical device and to comply with ISO 20957 and EN 957, and it must bear the required CE marking.