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Anbud

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

Lukket

Fristen for innlevering er utløpt

Fristen for innlevering av dette anbudet er utløpt og aksepterer ikke lenger søknader. Informasjonen nedenfor beholdes for referanseformål.

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Frist
Utløpt
10. februar 2026
Kontraktsdetaljer
Kategori
Varer
Referanse
304130
Verdi
€912,000
Sted
Estonia, Estland
Publisert
8. januar 2026
CPV-kode
Prosjektets tidslinje

Anbud publisert

8. januar 2026

Frist for spørsmål

3. februar 2026

Frist for innlevering

10. februar 2026

Anbudsåpning

10. februar 2026

Kontraktens startdato

2. mars 2026

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Budsjett
€912,000
Varighet
Ikke spesifisert
Sted
Estonia
Type
Varer
70
Kvalitetsscore/100
God
Markedsbenchmark
Gj.snittlig vinnerpris
€92,792
Gj.snittlig antall tilbud
2.2
Konkurranse
Lav
SMB-vinnere
86%
3,220 analyserte anbud

Opprinnelig anbudsbeskrivelse

Isedilateeruva supra-annulaarse aordiklapi ostmine väikeste klappide ja VIV jaoks
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Krav og kvalifikasjoner

20 krav på tvers av 5 kategorier

Innlevering (9)
Obligatorisk (1)
Overholdelse (4)
Teknisk (3)
Finansiell (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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Dokumenter

7 dokumenter tilgjengelig med AI-sammendrag

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.

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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.

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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.

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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.

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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.

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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.

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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
God

Anbudskvalitetsscore

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

Poengfordeling

Juridisk samsvar75/100

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)
Klarhet85/100

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.

Fullstendighet70/100

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
Rettferdighet45/100

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 gjennomførbarhet85/100

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
Bærekraft20/100

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

Styrker

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

Bekymringer

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

Anbefalinger

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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