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Anbud

Molekulaardiagnostika seadmed

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
oktober 06, 2025
Kontraktsdetaljer
Kategori
Varer
Referanse
299465
Verdi
€368,000
Sted
Estonia, Estland
Publisert
september 08, 2025
CPV-kode
Prosjektets tidslinje

Anbud publisert

september 08, 2025

Frist for spørsmål

september 29, 2025

Frist for innlevering

oktober 06, 2025

Anbudsåpning

oktober 06, 2025

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Budsjett
€368,000
Varighet
84 måneder
Sted
Estonia
Type
Varer
Markedsbenchmark
Gj.snittlig vinnerpris
€92,792
Gj.snittlig antall tilbud
2.2
Konkurranse
Lav
SMB-vinnere
86%
3,220 analyserte anbud

Opprinnelig anbudsbeskrivelse

Hangitakse Seegene Inc reaalaja-PCR reaktiivikomplektidega ühilduvaid reaalaja polümeraasi ahelreaktsiooni (edaspidi: reaalaja-PCR) seadmed koos vajalike tarvikute, hoolduse ja remondiga ning nukleiinhappe eraldusseade koos eraldusreaktiivide, tarvikute, hoolduse ja remondiga.
EU-finansiertElektronisk innlevering

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Vinnstrategi

Få en AI-drevet vinnerstrategi skreddersydd for dette anbudet. Inkluderer sannsynlighetsscore for å vinne, viktige muligheter og utfordringer, anbefalte fokusområder for tilbudet, innsikt i konkurranseposisjonering og handlingsrettede anbefalinger for å maksimere sjansene dine.

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Konkurrenter

Oppgrader for å se hvilke selskaper som sannsynligvis vil legge inn tilbud på dette anbudet, basert på historiske anskaffelsesdata.

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Krav og kvalifikasjoner

24 krav på tvers av 5 kategorier

Innlevering (4)
Obligatorisk (4)
Overholdelse (5)
Teknisk (5)
Finansiell (6)
SUBMISSION REQUIREMENTS4
--File the offer in Estonian (or with certified translation) before the stated deadline.
--Enclose Forms 1, 2 and 3 fully completed and signed.
--Attach CE certificates, Seegene compatibility evidence, prior installation report and verification protocol.
MANDATORY QUALIFICATIONS4
--Be the manufacturer or official distributor of CE-marked real-time PCR and nucleic-acid extraction devices that are already validated with Seegene reagents.
--Document at least one prior installation where the offered PCR and extraction units have been proven to run the eight specified Seegene Allplex kits (respiratory, GI, HPV, STI panels).
--Hold valid CE-IVD certification for all instruments and consumables offered.
COMPLIANCE REQUIREMENTS5
--Submit a single, non-conditional offer for the complete, indivisible lot—partial bids are automatically rejected.
--Sign and enclose Form 1 (participation confirmation) and, if applicable, Form 1 joint-bid power of attorney.
--Prove equivalence for any alternative standards or brands referenced in technical documentation.
TECHNICAL REQUIREMENTS5
--Supply real-time PCR instruments that are explicitly compatible with Seegene Inc reagents and a nucleic-acid extraction device that feeds the same workflow.
--Provide a detailed, page-numbered parts list showing every instrument module, accessory, computer, software version and required interface.
--Include a 6-year maintenance cost schedule and commit to 72- or 84-month full-service support (preventive maintenance, parts, labour, travel).
FINANCIAL REQUIREMENTS6
--Quote total lifecycle cost in euros, VAT excluded, on the official Excel cost-schedule (Vorm 3) covering:
--– Instruments and accessories
--– 7-year consumables package

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Dokumenter

10 dokumenter tilgjengelig med AI-sammendrag

VastavustingimusedPDF
299465_vastavustingimused.pdf -- 9.4 KB

This compliance document mandates that bidders submit a non-conditional offer confirming full adherence to all tender terms, provide pricing strictly in the prescribed Forms 2 & 3, prove equivalence for any referenced standards/brands, and—if bidding as a consortium—attach a joint-bid authorization, while forbidding the marking of price or numeric performance data as business secrets.

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Lisa 2. Tehniline kirjeldusDOC
Lisa 2 Tehniline kirjeldus- täiendatud.docx -- 32.1 KB

Viljandi Hospital is buying—only as a single, non-splittable lot—CE-marked Seegene-validated real-time PCR instruments and nucleic-acid extraction equipment that must be proven compatible with eight specified Seegene reagent kits; mandatory bid documents include a detailed parts list, 6-year maintenance cost schedule, 72- or 84-month service commitment, and precise page-numbered technical documentation, so only suppliers that already distribute Seegene-approved, CE-IVD systems and can price long-term service should bid.

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Vorm 2. Osalemise taotlusDOC
Vorm 1 Osalemise taotlus.docx -- 35.2 KB

This participation form merely requires bidders to confirm—without any technical or financial details—that they will supply, install and commission Seegene-compatible real-time PCR and nucleic-acid extraction devices as a single, sanctions-free turnkey package; no specific qualifications, experience or evaluation criteria are stated, so any firm able to source and integrate the specified equipment can consider bidding.

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Vorm 3. Maksumuse esildisXLS
Vorm 3 Maksumuse esildis-Täiendatud.xlsx -- 14.7 KB

This cost-schedule form (Vorm 3) requires bidders to price one mandatory nucleic-acid extraction device plus a 7-year consumables package (40 k extractions, 12–60 k PCR plates/tubes) in euros excluding VAT; no technical or qualification criteria are shown, so any supplier able to meet the volumes and quote the lowest compliant lifecycle cost should consider bidding.

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Hindamiskriteeriumid ja hinnatavad näitajadPDF
299465_hindamiskriteeriumid.pdf -- 2.8 KB

Viljandi Hospital is buying, in one non-divisible lot, real-time PCR instruments compatible with Seegene Inc reagents plus a nucleic-acid extraction device with all consumables, maintenance and repair; the award is 100 % price-based (lowest tax-excluded total wins) and bidders must simply submit a compliant offer that meets the technical/functional integration requirement.

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Hankepass täiendatavate selgitustegaPDF
299465_hankepass_taiendavate_selgitustega.pdf -- 66.6 KB

Viljandi Hospital is buying, in a single non-divisible lot, Seegene-compatible real-time PCR instruments plus nucleic-acid extraction equipment complete with reagents, accessories and full-service maintenance—bidders must therefore prove they can supply this specific integrated workflow (technical compatibility is mandatory) and meet the standard ESPD qualification checks (no special financial or experience thresholds stated).

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Hanke alusdokumentDOC
Hanke alusdokument.docx -- 61.0 KB

This open procurement by SA Viljandi Haigla seeks a single-lot supply of real-time PCR devices compatible with Seegene Inc reagents and a nucleic-acid extraction unit, all with consumables, service and repair; mandatory compliance with technical/functional integration is required, but specific qualifications, delivery terms and award criteria are not stated in the released excerpt.

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Lisa 1. Hankelepingu projektDOC
Lisa 1 Hankelepingu kavand_molekulaardiagnost... -- 33.7 KB

Viljandi Hospital is buying as a single lot (no partial bids) Seegene-compatible real-time PCR instruments plus nucleic-acid extraction devices, each with full reagents, accessories and 5-year service; bidders must therefore supply and integrate both systems, provide Estonian-language support and warranty, and show prior Seegene compatibility experience—mandatory requirements, so only vendors that can deliver the complete validated workflow should bid.

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VerifitseerimisplaanDOC
Verifitseerimisplaan.docx -- 55.9 KB

This verification plan mandates that suppliers of real-time PCR and nucleic-acid extraction equipment must prove—within 45 days of installation and user training—full technical compatibility with eight specified Seegene Allplex reagent kits (respiratory, GI, HPV, STI panels) through prospective on-site verification, making prior Seegene experience and documented integration capability essential for any bidder.

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Vorm 1. VolikiriDOC
Vorm 1 Ühispakkujate volikiri.docx -- 14.8 KB

This document is merely the blank “Form 1 – Joint-bid Power of Attorney” for the Viljandi Hospital Foundation tender “Molekulaardiagnostica equipment”; it contains no technical requirements, qualification criteria or evaluation rules—only spaces for lead and member bidders to fill in their names, reg. codes, addresses and e-mails when submitting a joint offer.

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Kvalitetsscore

Omfattende kvalitetsanalyse av dette anbudet som vurderer juridisk samsvar, klarhet, fullstendighet, rettferdighet, praktisk gjennomførbarhet, datakonsistens og bærekraft på en skala fra 0-100 med detaljert oversikt og anbefalinger.

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