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Upphandlingar

Self-dilating supra-annular aortic valve for small valves and VIV

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Utgånget
10 februari 2026
Avtalsdetaljer
Kategori
Leveranser
Referens
304130
Värde
€912,000
Plats
Estonia, Estland
Publicerad
8 januari 2026
CPV-kod
Tidsplan för projektet

Upphandling publicerad

8 januari 2026

Sista dag för frågor

3 februari 2026

Sista anbudsdag

10 februari 2026

Anbudsöppning

10 februari 2026

Avtalets startdatum

2 mars 2026

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Budget
€912,000
Varaktighet
Ej angivet
Plats
Estonia
Typ
Leveranser
70
Kvalitetspoäng/100
Bra
Marknadsjämförelse
Genomsnittligt vinnande pris
€92,792
Genomsnittligt antal anbud
2.2
Konkurrens
Låg
Vinnande små och medelstora företag
86%
3,220 analyserade upphandlingar

Ursprunglig beskrivning av upphandling

Isedilateeruva supra-annulaarse aordiklapi ostmine väikeste klappide ja VIV jaoks
Elektronisk inlämning

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Vinnande strategi

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Konkurrenter

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Krav och kvalifikationer

20 krav inom 5 kategorier

Inlämning (9)
Obligatorisk (1)
Regelefterlevnad (4)
Teknisk (3)
Ekonomisk (3)
SUBMISSION REQUIREMENTS9
--Tenders must be submitted by the deadline: 2026-02-10 12:00:00.
--Bidders must adhere to the specified formats for submitting a tender proposal.
--Bidders must submit all necessary supporting documents.
MANDATORY EXCLUSION GROUNDS1
--Bidders must meet the mandatory exclusion criteria outlined by the contracting authority in the European Single Procurement Document (ESPD).
ELIGIBILITY REQUIREMENTS4
--Bidders must meet the qualification criteria outlined by the contracting authority in the European Single Procurement Document (ESPD).
--Bidders must meet the mandatory conditions for submitting a tender proposal.
--Bidders must be able to supply catheter-implantable aortic valves and their installation tools.
TECHNICAL CAPABILITY REQUIREMENTS3
--The offered transcatheter aortic valves (TAVI) and related equipment must comply with the detailed technical specifications.
--Bidders must be prepared for the process of testing offered products.
--Bidders must provide product codes, names, technical parameters, and manufacturer details for the offered self-dilating supra-annular aortic valves.
FINANCIAL REQUIREMENTS3
--Bidders must structure their costs according to the specified cost structure requirements.
--The tender price must account for all costs and obligations.
--Bids will be evaluated solely on the total cost (excluding VAT), with the lowest price receiving the maximum points.

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Dokument

7 dokument tillgängliga med AI-sammanfattningar

VastavustingimusedPDF
304130_vastavustingimused.pdf -- 7.2 KB

This document outlines the mandatory conditions and formats for submitting a tender proposal, including technical requirements, cost structure, necessary supporting documents, and rules for joint bids.

Ettevõtja esitab täidetud maksumuse vormiXLS
304130 maksumuse vorm.xlsx -- 14.1 KB

This is a mandatory cost form for submitting product codes, names, technical parameters, manufacturer details, quantities, unit prices, and total costs for the offered self-dilating supra-annular aortic valves.

Ettevõtja esitab täidetud pakkumuse vormiDOC
304130 tehniline kirjeldus.docx -- 52.6 KB

This document details the technical specifications for transcatheter aortic valves (TAVI) and related equipment, along with instructions for tender submission and the process for testing offered products.

Ettevõtja kinnitab, et täidab kõik hankemenetluse osalemise avalduses toodud tin...DOC
Hankemenetluses osalemise avaldus.docx -- 50.7 KB

This document is a tender submission application where the bidder confirms having reviewed and accepted the procurement terms, and has accounted for all costs and obligations in the tender price.

Hindamiskriteeriumid ja hinnatavad näitajadPDF
304130_hindamiskriteeriumid.pdf -- 3.1 KB

This document outlines the tender's evaluation criteria, stating that the total cost (excluding VAT) is the sole criterion with a 100% weighting, where the lowest price receives the maximum points.

Hankepass täiendatavate selgitustegaPDF
304130_hankepass_taiendavate_selgitustega.pdf -- 62.9 KB

This document serves as an explanatory guide to the European Single Procurement Document (ESPD), outlining the contracting authority's qualification and exclusion criteria for bidders, but it is for informational purposes only and not for submission.

Raamlepingu projektDOC
304130 raamlepingu projekt.docx -- 50.6 KB

This document is a draft framework agreement outlining the terms for the supply and sale of catheter-implantable aortic valves and their installation tools to SA Põhja-Eesti Regionaalhaigla until November 30, 2027, with a possibility of extension.

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70
Bra

Upphandlingskvalitetspoäng

Overall, the tender is well-structured with clear evaluation criteria, but significant concerns arise from the ambiguous procedure type and severely limited competition.

Poängfördelning

Regelefterlevnad75/100

The tender demonstrates compliance with general legal frameworks, including reasonable submission deadlines and proper CPV code assignment. However, the procedure type is ambiguously defined as 'Type: A' and 'Procedure: A' with N/A codes, which is a notable deviation from standard procurement terminology.

•Ambiguous procedure type ('Type: A', 'Procedure: A' with N/A codes)
Tydlighet85/100

The tender's description is specific, and requirements are comprehensively detailed across various categories. The evaluation criteria, based solely on the lowest total cost (excluding VAT) with 100% weighting, are exceptionally clear and unambiguous.

Fullständighet70/100

Most essential information, including title, organization, reference, financial details, and deadlines, is provided. While the framework agreement duration is specified, a distinct 'contract duration' field could be clearer. One XML document was listed but not analyzed by AI, representing a minor gap in content processing.

•Contract duration could be more explicitly defined as a single field
•One XML document not analyzed by AI
Rättvisa45/100

The 'Max Participants: 1' characteristic, combined with the highly specialized nature of the product and the explicit statement that the procurement is not divided into parts, raises significant concerns about severely limited competition and potential tailoring of requirements. While evaluation criteria are objective (lowest price), the restricted pool of potential bidders compromises fairness.

•'Max Participants: 1' severely limits competition
•Highly specialized product not divided into lots, further restricting competition
Praktisk genomförbarhet85/100

The tender supports electronic submission and e-procurement, enhancing accessibility. Key dates such as the contract start date and financing information are clearly provided, contributing to practical execution.

Datakonsistens80/100

Dates and financial figures are logical and consistent throughout the tender. The primary inconsistency lies in the non-standard and ambiguous 'Type: A' and 'Procedure: A' codes for the procurement process.

•Non-standard and ambiguous procedure type codes
Hållbarhet20/100

The tender lacks any explicit criteria or focus on green procurement, social aspects, or innovation. This is a common omission in highly specialized medical device procurements but results in a low score for this category.

•No green procurement criteria
•No social aspects included

Styrkor

Clear and objective evaluation criteria (100% lowest price)
Comprehensive AI-extracted requirements covering key aspects
Strong support for electronic submission and e-procurement
Reasonable submission deadline for preparation
Detailed technical specifications and draft framework agreement provided

Potentiella problem

Ambiguous procurement procedure type ('Type: A', 'Procedure: A' with N/A codes)
'Max Participants: 1' raises significant concerns about limited competition and potential tailoring
Highly specialized product not divided into lots, further restricting competition
Lack of explicit sustainability, social, or innovation criteria
One XML tender document not analyzed by AI, potentially hiding details

Rekommendationer

1. Clearly define the procurement procedure type using standard, recognized terminology.
2. Provide a robust justification for 'Max Participants: 1' and the decision not to divide the procurement into lots, demonstrating thorough market research to ensure fair competition.
3. Consider incorporating sustainability, social, or innovation criteria where feasible, even for specialized medical devices, to align with broader public procurement goals.

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