Bulgaria – Medical equipments – Доставка на високоспециализирани пациентни монитори с мониторна станция за Клиника по кардиология при УМБАЛ „Света Анна“ – София АД.

The public procurement contract covers the delivery of highly specialised patient monitors with a monitoring station for the Cardiology Clinic at UMBAL "Sveta Anna" – Sofia AD. The medical equipment must fully comply with the requirements and technical characteristics specified in the specification prepared by the Contracting Authority. The scope of the contract includes the following activities: delivery, installation, commissioning, training of personnel to work with the equipment, and warranty support for 8 (eight) highly specialised patient monitors with 1 (one) monitoring station for the Cardiology Clinic at UMBAL "Sveta Anna" – Sofia AD. Participants submit only one offer for the comprehensive execution of the contract, and the submission of variants is not allowed. The declaration period for the medical equipment is 12 months, with execution taking place after a written request, depending on the needs of the Contracting Authority. The delivery period for the equipment is proposed by the participant in calendar days, not exceeding 90 calendar days from the submission of a written request. The healthcare facility has no obligation to purchase the medical equipment, which is the subject of this procedure. The warranty period for the medical equipment is proposed by the participant, in months, and cannot be less than 24 (twenty-four) months from the date of the acceptance protocol for completed delivery. Payment is made in euros, by bank transfer, deferred, within a period proposed by the participant, but not less than 60 calendar days after the submission of a written request, invoice, warranty card, and acceptance protocol. The final price includes all costs to the ultimate recipient UMBAL "Sveta Anna" – Sofia AD. Each participant must attach the following documents to their technical proposal, which are an integral part of it: 1. Technical documents, brochures, and catalogs from which the parameters of the medical equipment offered by the participant and its compliance with the requirements of the Contracting Authority, listed in the technical specification, are visible. 2. An authorization letter from the manufacturer of the medical equipment or their authorized representative with the right of the participant to trade in their products. An authorization letter is not required only in cases where the participant and the manufacturer are the same entity.