Supply of single-use medical devices for the needs of the Pulmonology and Toracosurgery Centre in Bystra (repetition of cancelled Packages)

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20/Dz.ZP/380/APT/4/2026

The subject of the order is the supply of single-use medical devices for the needs of the Pulmonology and Toracosurgery Center in Bystra (repetition in the scope of invalidated packages), a detailed description of the subject of the order in the assortment and quantities has been specified in the assortment and price form - Annex No 2 to the SWZ. The order consists of 26 packages. It is allowed to submit partial offers for individual Packages (one or several), as part of individual Packages it is required to submit an offer for the full scope of the subject of the contract related to a given Package. The expiry date of the offered assortment is required at least 6 months from the moment of delivery of the order to the Ordering Party, unless a different expiry date is indicated in Annex 2 to the SWZ. The customer requires that the entire assortment be new and unused. All offered medical materials that are medical devices must be placed on the market and used in the territory of the Republic of Poland, classified according to the applicable regulations: Regulation (EU) 2017/745 on medical devices, Regulation (EU) 2017/746 on in vitro diagnostic medical devices, Act of 7 April 2022 on medical devices (Journal of Laws 2022, No. U. 2024, item 1620) to which it applies. Offered medical devices should have the manufacturer's EU declarations of conformity and, in the case of classes of devices higher than 1st class, certificates of conformity issued by a notified body authorised to certify under the MDR/MDD regulations. If an extended transition period is used (invalid certificate, certificate issued under the ‘old’ directives: 90/385/EEC or Directive 93/42/EEC) in connection with the need to confirm that the offered medical device may be placed on the market under the transitional provisions, a statement on the use of the transitional period, the manufacturer's self-declaration specifying the date of the end of the transitional period, the manufacturer's quality management system certificate, confirmation of the conclusion of the contract for conformity assessment of the device with a notified body. Products offered must be CE marked, have instructions for use in Polish and be marked with the name / trade name or registered trademark, the address of the manufacturer's registered place of business. If the registered place of business is outside the EU, they shall have the name of the authorised representative and the address of his registered place of business. The requirements for the subject of the contract are indicated in section. II FTZ para. 1 Subject of the contract, in Annex No 2 to the SPC - product and price form and in Annex No 7 to the SPC - draft contract. The Contractor will be bound by the offer until 08.12.2026 (90 days),

Electronic via:
https://szpitalbystra.logintrade.net/zapytania_email,237153,18c360243e76fd35e85ecc67e269c010.html

Electronic submission: required
https://szpitalbystra.logintrade.net/zapytania_email,237153,18c360243e76fd35e85ecc67e269c010.html

Not available

10/09/2026 09:15

PL225 Bielski
PL Polska

33141000 - Disposable non-chemical medical consumables and haematological consumables

33141900 - Blood lancets

33157200 - Oxygen kits

33141320 - Medical needles

33140000 - Medical consumables

33141220 - Cannulae

33141323 - Biopsy needles

33141642 - Drain accessories

33141300 - Venepuncture, blood sampling devices

33141200 - Catheters

33141310 - Syringes

33141640 - Drain

33171110 - Anaesthesia mask

33196000 - Medical aids

33190000 - Miscellaneous medical devices and products