Koronar- und Gefäßstents sowie Embolieschutzsysteme für die interventionelle Kardiologie

Status
Offen
Angebotsfrist
23.11.2026, 12:00 (Europe/Berlin)
Geschätzter Wert
Nicht angegeben
Lose
26
Erfüllungsregion
MK008, MKD
Verfahren
Offenes Verfahren
Auftragsart
Lieferleistung
Veröffentlicht
27.10.2026
CPV-Codes
Medizinische Ausrüstungen, Arzneimittel und Körperpflegeprodukte (33000000)
Bekanntmachung
e-nabavki.gov.mk
Bekanntmachungsnummer
743838-2026
Verfahrensnummer
801467d5-febf-42e5-af66-9f002a26b6e1

Fragenkatalog

Deine Fragen an die Ausschreibung, beantwortet aus Bekanntmachung und Unterlagen.

Kurzbeschreibung

Die PHI UNIVERSITY CLINIC FOR CARDIOLOGY AND CARDIOVASCULAR SURGERY NATIONAL CENTER FOR CARDIOVASCULAR DISEASES in Skopje schreibt in 26 Losen Stents und medizinische Verbrauchsmaterialien für die interventionelle Kardiologie aus. Dazu gehören unter anderem Koronar-, Karotis- und periphere Stents sowie Systeme zum Schutz vor distalen Embolien; die Laufzeit der Lose beträgt jeweils 360 Tage. Der Auftrag wird in Nordmazedonien ausgeführt, die Angebotsfrist endet am 23. November 2026.

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Leistungsbeschreibung

Medical devices and medical consumables for interventional cardiology – stents and distal embolic protection.

Leistungen nach Losen (26)

  • LOT-0001 · Medical devices and medical consumables for interventional cardiology – stents and distal embolic protection.

    Medical devices and medical consumables for interventional cardiology – stents and distal embolic protection.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0002 · Coronary stent with a sinusoidal configuration and a permanent polymer coating containing a cytostatic agent from the “-limus” family (DES), with a platinum-iridium core for enhanced radiopacity, an outer cobalt-chromium layer, and platinum-iridium markers; minimum stent diameter range 2.25–4.0 mm and minimum length range 8–38 mm.

    Coronary stent with a sinusoidal configuration and a permanent polymer coating containing a cytostatic agent from the “-limus” family (DES), with a platinum-iridium core for enhanced radiopacity, an outer cobalt-chromium layer, and platinum-iridium markers; minimum stent diameter range 2.25–4.0 mm and minimum length range 8–38 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0003 · Coronary stent with a permanent polymer coating containing a cytostatic agent from the LIMUS family (DES), with a platinum-iridium core for enhanced radiopacity, an outer cobalt-chromium layer, and platinum-iridium markers; minimum stent diameter range 2.0–5.00 mm, with overexpansion capability up to 6.00 mm (for 4.5–5.0 mm diameters), and a minimum length range of 8–38 mm.

    Coronary stent with a permanent polymer coating containing a cytostatic agent from the LIMUS family (DES), with a platinum-iridium core for enhanced radiopacity, an outer cobalt-chromium layer, and platinum-iridium markers; minimum stent diameter range 2.0–5.00 mm, with overexpansion capability up to 6.00 mm (for 4.5–5.0 mm diameters), and a minimum length range of 8–38 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0004 · Coronary stent designed for the treatment of large-lumen blood vessels, with high radial and axial strength, made of platinum-chromium alloy, abluminally coated with a bioresorbable PLGA polymer and the cytostatic agent everolimus (DES), with a dual-layer balloon system, a diameter range of 3.5–5 mm, and a length range of 8–32 mm. The stent can be further expanded up to a maximum diameter of 6 mm.

    Coronary stent designed for the treatment of large-lumen blood vessels, with high radial and axial strength, made of platinum-chromium alloy, abluminally coated with a bioresorbable PLGA polymer and the cytostatic agent everolimus (DES), with a dual-layer balloon system, a diameter range of 3.5–5 mm, and a length range of 8–32 mm. The stent can be further expanded up to a maximum diameter of 6 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0005 · Coronary stent made of platinum-chromium alloy, with a thin stent strut profile ≤81 μm, a non-linear link design with an open-cell configuration, abluminally coated with a bioresorbable PLGA polymer and the cytostatic agent everolimus (DES), with a dual-layer balloon system, a diameter range of 2.25–5 mm, and a length range of 8–48 mm, compatible with a 5F guiding catheter for all sizes.

    Coronary stent made of platinum-chromium alloy, with a thin stent strut profile ≤81 μm, a non-linear link design with an open-cell configuration, abluminally coated with a bioresorbable PLGA polymer and the cytostatic agent everolimus (DES), with a dual-layer balloon system, a diameter range of 2.25–5 mm, and a length range of 8–48 mm, compatible with a 5F guiding catheter for all sizes.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0006 · Self-expanding cobalt-chromium stent for carotid arteries, compatible with a 0.014" guidewire and a 5F introducer sheath, with a straight and tapered closed-cell design, a diameter range of 6–10 mm, and a length range of 30–50 mm.

    Self-expanding cobalt-chromium stent for carotid arteries, compatible with a 0.014" guidewire and a 5F introducer sheath, with a straight and tapered closed-cell design, a diameter range of 6–10 mm, and a length range of 30–50 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0007 · Coronary stent made of cobalt-chromium alloy, with an open-cell design and a biodegradable polymer coating, coated with the immunosuppressive drug sirolimus, with a stent strut thickness of 60 µm, featuring PROBIO coating (amorphous silicon carbide), a diameter range of 2.25–4 mm, and a length range of 9–40 mm.

    Coronary stent made of cobalt-chromium alloy, with an open-cell design and a biodegradable polymer coating, coated with the immunosuppressive drug sirolimus, with a stent strut thickness of 60 µm, featuring PROBIO coating (amorphous silicon carbide), a diameter range of 2.25–4 mm, and a length range of 9–40 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0008 · Peripheral balloon-expandable stent, made of cobalt-chromium, with an OTW (over-the-wire) system, compatible with a 6F introducer sheath, with a strut thickness of 110 µm (for stents with diameters of 5–7 mm), featuring PROBIO coating, with 2 markers, on a 90, 135, and 170 cm delivery catheter, with a stent length range of 18–78 mm and a diameter range of 5–10 mm.

    Peripheral balloon-expandable stent, made of cobalt-chromium, with an OTW (over-the-wire) system, compatible with a 6F introducer sheath, with a strut thickness of 110 µm (for stents with diameters of 5–7 mm), featuring PROBIO coating, with 2 markers, on a 90, 135, and 170 cm delivery catheter, with a stent length range of 18–78 mm and a diameter range of 5–10 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0009 · Coronary stent made of cobalt-chromium alloy, with a non-linear multi-link cell design, coated with a permanent polymer and the cytostatic agent everolimus (DES), with a diameter range of 2–4 mm and a length range of 8 mm to at least 38 mm, compatible with a 5F guiding catheter for all sizes.

    Coronary stent made of cobalt-chromium alloy, with a non-linear multi-link cell design, coated with a permanent polymer and the cytostatic agent everolimus (DES), with a diameter range of 2–4 mm and a length range of 8 mm to at least 38 mm, compatible with a 5F guiding catheter for all sizes.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0010 · Coronary stent made of cobalt-chromium alloy, with a multi-link, non-linear link stent design, intended for large-diameter coronary arteries, coated with a permanent polymer and the cytostatic agent everolimus (DES), with a low stent crossing profile of ≤0.039" (for a 3 mm stent diameter), a diameter range of 2.25–4 mm, and a length range of 8–38 mm, with expansion capability up to 5.5 mm for 3.5

    Coronary stent made of cobalt-chromium alloy, with a multi-link, non-linear link stent design, intended for large-diameter coronary arteries, coated with a permanent polymer and the cytostatic agent everolimus (DES), with a low stent crossing profile of ≤0.039" (for a 3 mm stent diameter), a diameter range of 2.25–4 mm, and a length range of 8–38 mm, with expansion capability up to 5.5 mm for 3.5 and 4.0 mm diameters without shortening, compatible with a 5F guiding catheter for all sizes.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0011 · Peripheral nitinol stent system, self-expanding, with a woven mesh design, flexible and kink-resistant, intended for interventions in the femoral and popliteal arteries, with a diameter range of 4.5–7.5 mm and a stent length range of 20–200 mm, compatible with a 6F introducer sheath.

    Peripheral nitinol stent system, self-expanding, with a woven mesh design, flexible and kink-resistant, intended for interventions in the femoral and popliteal arteries, with a diameter range of 4.5–7.5 mm and a stent length range of 20–200 mm, compatible with a 6F introducer sheath.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0012 · Self-expanding carotid stent system made of nitinol alloy, with a closed-cell design, an RX system, with a straight or tapered diameter ranging from 6.0 to 10.0 mm and lengths ranging from 20 to 40 mm, compatible with a 6F guiding introducer sheath.

    Self-expanding carotid stent system made of nitinol alloy, with a closed-cell design, an RX system, with a straight or tapered diameter ranging from 6.0 to 10.0 mm and lengths ranging from 20 to 40 mm, compatible with a 6F guiding introducer sheath.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0013 · Distal embolic protection system for carotid artery stenting, featuring technology for independent deployment of a 0.014" guidewire, three levels of wire support, and subsequent deployment of an embolic protection filter with diameters of 5 and 7.2 mm and pore size of at least 120 µm; the system includes a retrieval catheter and is fully compatible with a 6F introducer sheath or a 7F guiding cathe

    Distal embolic protection system for carotid artery stenting, featuring technology for independent deployment of a 0.014" guidewire, three levels of wire support, and subsequent deployment of an embolic protection filter with diameters of 5 and 7.2 mm and pore size of at least 120 µm; the system includes a retrieval catheter and is fully compatible with a 6F introducer sheath or a 7F guiding catheter.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0014 · Coronary CoCr DES stent designed for long, complex, and bifurcation lesions, coated with a bioresorbable polymer containing a cytostatic agent from the “LIMUS” family, selectively applied to the abluminal surface at 3.9 μg/mm, with an open-cell design, a diameter range of 2.0–4.5 mm, and a length range of 9–50 mm.

    Coronary CoCr DES stent designed for long, complex, and bifurcation lesions, coated with a bioresorbable polymer containing a cytostatic agent from the “LIMUS” family, selectively applied to the abluminal surface at 3.9 μg/mm, with an open-cell design, a diameter range of 2.0–4.5 mm, and a length range of 9–50 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0015 · Self-expanding carotid stent made of nitinol alloy, with a flexible, dual-layer micromesh closed-cell design for protection against embolization, with repositioning capability during deployment up to 50%, compatible with a 5F introducer sheath and an RX system, with a stent diameter range of 5–10 mm and a stent length range of 16–40 mm.

    Self-expanding carotid stent made of nitinol alloy, with a flexible, dual-layer micromesh closed-cell design for protection against embolization, with repositioning capability during deployment up to 50%, compatible with a 5F introducer sheath and an RX system, with a stent diameter range of 5–10 mm and a stent length range of 16–40 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0016 · Peripheral stent-graft system, balloon-expandable, indicated for interventions in the renal and/or iliac arteries, consisting of a stainless-steel stent with an open-cell design, fully encapsulated in a single PTFE layer with a controlled pore size of 55 µm, with a diameter range of 5–10 mm and a length range of 16–59 mm, compatible with a 6–7F introducer sheath and a 0.035" guidewire, with cathet

    Peripheral stent-graft system, balloon-expandable, indicated for interventions in the renal and/or iliac arteries, consisting of a stainless-steel stent with an open-cell design, fully encapsulated in a single PTFE layer with a controlled pore size of 55 µm, with a diameter range of 5–10 mm and a length range of 16–59 mm, compatible with a 6–7F introducer sheath and a 0.035" guidewire, with catheter lengths of 80 and 120 cm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0017 · Coronary stent-graft system, balloon-expandable, made of cobalt-chromium alloy, intended for the management of complications during interventions, with a maximum profile of 1.25 mm, compatible with a 5F catheter for diameters of 2.5–4.0 mm and a 6F catheter for diameters of 4.5 and 5.0 mm, with lengths ranging from 15 to 26 mm.

    Coronary stent-graft system, balloon-expandable, made of cobalt-chromium alloy, intended for the management of complications during interventions, with a maximum profile of 1.25 mm, compatible with a 5F catheter for diameters of 2.5–4.0 mm and a 6F catheter for diameters of 4.5 and 5.0 mm, with lengths ranging from 15 to 26 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0018 · Peripheral stent-graft system with high radial strength, indicated for implantation in the iliac and renal arteries for the treatment of aneurysms, acute perforations, acute ruptures, and fistulas. Made of a cobalt-chromium (CoCr) stent covered with a 203 μm ePTFE layer. Balloon-expandable, with a 5F shaft, compatible with a 0.035" guidewire, with diameters ranging from 5–10 mm, lengths ranging fr

    Peripheral stent-graft system with high radial strength, indicated for implantation in the iliac and renal arteries for the treatment of aneurysms, acute perforations, acute ruptures, and fistulas. Made of a cobalt-chromium (CoCr) stent covered with a 203 μm ePTFE layer. Balloon-expandable, with a 5F shaft, compatible with a 0.035" guidewire, with diameters ranging from 5–10 mm, lengths ranging from 18–58 mm, and catheter lengths of 75 cm and 120 cm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0019 · Balloon-expandable covered peripheral stent with a dual ePTFE layer, inner and outer. Made of CoCr alloy, with an open-cell design, featuring three radiopaque markers at each end of the stent and two markers on the balloon. Diameter range: 5–10 mm; length range: 17–57 mm; compatible with a 0.035" guidewire. Catheter lengths: 80 and 140 cm.

    Balloon-expandable covered peripheral stent with a dual ePTFE layer, inner and outer. Made of CoCr alloy, with an open-cell design, featuring three radiopaque markers at each end of the stent and two markers on the balloon. Diameter range: 5–10 mm; length range: 17–57 mm; compatible with a 0.035" guidewire. Catheter lengths: 80 and 140 cm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0020 · Self-expanding carotid stent made of nitinol, featuring technology designed to prevent plaque prolapse through the stent for permanent embolic protection, with a dual-layer design and an open-cell configuration, with a diameter range of 6–10 mm and a length range of 20–60 mm (for selected diameters).

    Self-expanding carotid stent made of nitinol, featuring technology designed to prevent plaque prolapse through the stent for permanent embolic protection, with a dual-layer design and an open-cell configuration, with a diameter range of 6–10 mm and a length range of 20–60 mm (for selected diameters).

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0021 · Coronary bioadaptor – coronary scaffold composed of three CoCr sinusoidal arrays, coated with a drug and a bioresorbable polymer, designed to unlock the scaffold six months after implantation; diameter range: 2.25–4.0 mm; length range: 14–38 mm.

    Coronary bioadaptor – coronary scaffold composed of three CoCr sinusoidal arrays, coated with a drug and a bioresorbable polymer, designed to unlock the scaffold six months after implantation; diameter range: 2.25–4.0 mm; length range: 14–38 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0022 · Coronary stent system (DES) with everolimus, featuring an ultrathin 50 µm cobalt-chromium L605 platform, coated with a biodegradable and biocompatible polymer that delivers everolimus (LIMUS family) for controlled drug release, with a hybrid cell design, equipped with platinum-iridium radiopaque markers, a rapid-exchange delivery system compatible with a 0.014" guidewire and a 5F guiding catheter,

    Coronary stent system (DES) with everolimus, featuring an ultrathin 50 µm cobalt-chromium L605 platform, coated with a biodegradable and biocompatible polymer that delivers everolimus (LIMUS family) for controlled drug release, with a hybrid cell design, equipped with platinum-iridium radiopaque markers, a rapid-exchange delivery system compatible with a 0.014" guidewire and a 5F guiding catheter, with diameters ranging from 2.00–4.50 mm and lengths ranging from 8–48 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0023 · Dedicated bifurcation stent system for side branches, with sirolimus (DES) on a 65 µm cobalt-chromium L605 platform, featuring a biodegradable polymer coating (PLGA + PLLA) for controlled drug release (~30 days), with a main-branch anchoring segment with markers for positioning at the carina and ostium (4 platinum-iridium markers), a rapid-exchange delivery system with a step balloon, compatible w

    Dedicated bifurcation stent system for side branches, with sirolimus (DES) on a 65 µm cobalt-chromium L605 platform, featuring a biodegradable polymer coating (PLGA + PLLA) for controlled drug release (~30 days), with a main-branch anchoring segment with markers for positioning at the carina and ostium (4 platinum-iridium markers), a rapid-exchange delivery system with a step balloon, compatible with a 0.014" guidewire and a 5F guiding catheter, available in diameter combinations ranging from 2.50–2.50 mm to 4.00–3.50 mm and lengths ranging from 16–29 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0024 · Tapered stent system for the treatment of long, diffuse lesions using a single stent. Stent material: cobalt-chromium L605 alloy or equivalent; stent strut thickness: 65 µm; drug (active substance): sirolimus; polymer: biodegradable and biocompatible; delivery system: Rapid Exchange (RX) system; drug dose: 1.25 µg/mm². Diameter combinations: 2.75–2.25 mm, 3.00–2.50 mm, 3.50–2.75 mm, and 3.50–3.00

    Tapered stent system for the treatment of long, diffuse lesions using a single stent. Stent material: cobalt-chromium L605 alloy or equivalent; stent strut thickness: 65 µm; drug (active substance): sirolimus; polymer: biodegradable and biocompatible; delivery system: Rapid Exchange (RX) system; drug dose: 1.25 µg/mm². Diameter combinations: 2.75–2.25 mm, 3.00–2.50 mm, 3.50–2.75 mm, and 3.50–3.00 mm; length range: 30–60 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0025 · Cobalt-chromium alloy coronary stent, multi-link, featuring a Peak-to-Valley stent design for the treatment of tapered (conically narrowed) coronary lesions with small and large diameters, coated with a permanent polymer and the cytostatic drug everolimus (DES), with a strut thickness of 81 µm, a diameter range of 2 to 5 mm, and lengths ranging from 8 to 48 mm, with the capability of expansion up

    Cobalt-chromium alloy coronary stent, multi-link, featuring a Peak-to-Valley stent design for the treatment of tapered (conically narrowed) coronary lesions with small and large diameters, coated with a permanent polymer and the cytostatic drug everolimus (DES), with a strut thickness of 81 µm, a diameter range of 2 to 5 mm, and lengths ranging from 8 to 48 mm, with the capability of expansion up to 5.75 mm for diameters of 3.5–5.0 mm and expansion up to 3.75 mm for diameters of 2.0–3.25 mm without shortening.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

  • LOT-0026 · Peripheral CoCr stent for BTK calcified arteries, coated with sirolimus at 1.4 μg/mm² and a fluoroacrylate trilayer coating, with drug release over 2 months (75% during the first month), open-cell design with alternating links, strut thickness of 75–85 µm, high radial strength, shortening of <3%, pre-mounted on an Rx semi-compliant balloon with a 142 cm catheter, hydrophilic coating, tip profile o

    Peripheral CoCr stent for BTK calcified arteries, coated with sirolimus at 1.4 μg/mm² and a fluoroacrylate trilayer coating, with drug release over 2 months (75% during the first month), open-cell design with alternating links, strut thickness of 75–85 µm, high radial strength, shortening of <3%, pre-mounted on an Rx semi-compliant balloon with a 142 cm catheter, hydrophilic coating, tip profile of 0.016", crossing profile of 0.043"–0.051", compatible with a 0.014" guidewire and a 5F guiding catheter. Dimensions: diameter 2.0–4.5 mm; length 9–39 mm.

    Frist: 23.11.2026, 01:00 (Europe/Berlin)

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