Poland - Laboratory, optical and precision equipment (excluding glassware)

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Details

Provided by Open Opps
Opportunity closing date
20 September 2021
Opportunity publication date
23 August 2021
Category
38000000: La
Value of contract
to be confirmed
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Description

The subject matter of the contract is the supply of laboratory equipment for the implementation of the project entitled: "Genetically conditioned diseases - education and diagnostics". A detailed description of the subject matter of the contract is attached as Annex No. 2 and 3 to the SWZ.The Ordering Party declares that, being a data controller and having regard to the provisions of the Act of 10 May 2018 on the protection of personal data (hereinafter referred to as "RODO"), it has implemented security measures adequate to the risks identified by it and giving guarantees of proper protection of personal data provided within the proceedings. The detailed information clause in Article 13 of RODO is included in the SWZ.
Centrifuge without cooling. The Ordering Party demands submitting, together with the offer, under pain of invalidity, in an electronic form, the following means of evidence to confirm that the offered supplies meet the requirements specified by the Ordering Party on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document confirming notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device is compliant with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires a statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the Contractor shall only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosures 2 and 3 to SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority accepts submission of the documents mentioned in item 2) in English.2. If the Economic Operator does not submit such evidence or if the submitted evidence is incomplete, the Contracting Authority will call for its submission or supplementation within the established time limit. Laboratory balance. A detailed description of the subject matter of the contract is enclosed as Attachment No. 2 to the SWZ - Assortment and Price Table.1The Contracting Authority demands that the following means of proof be submitted together with the offer, under pain of invalidity, in an electronic form, to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate issued by an entity authorised to control quality, confirming that the supplied products meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 2 to the SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or if the submitted evidence is incomplete, the Contracting Authority shall call for its submission or completion within the prescribed time limit. Microwave oven. A detailed description of the subject matter of the contract is enclosed as appendix no. 2 to the SWZ - the assortment and price table.1The Contracting Authority demands that the following means of proof be submitted together with the tender under pain of invalidity, in an electronic form, to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the supplied products meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 2 to the SWZ (indicating the required parameters, part No. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or the submitted evidence is incomplete, the Contracting Authority shall call for its submission or supplementation within the prescribed time limit. Shredder type I. A detailed description of the subject matter of the contract is enclosed as Attachment No. 3 to the SWZ - Description of the Subject Matter of the Contract.1The Contracting Authority demands that the following means of proof be submitted with the tender under pain of invalidity, in electronic form, to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the supplied products conform to certain harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part No. and position of the offered subject matter of the contract).NOTE: The Contracting Authority accepts submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or the submitted evidence is incomplete, the Contracting Authority shall call for its submission or supplementation within the prescribed time limit. Type II extruder. A detailed description of the subject matter of the contract is enclosed as Attachment No. 3 to the SWZ - Description of the subject matter of the contract.1The Contracting Authority demands that the following means of proof be submitted with the tender under pain of invalidity, in electronic form, to confirm that the supplies offered meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the products supplied meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows the submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or if the submitted evidence is incomplete, the Contracting Authority shall call for its submission or supplementation within the prescribed time limit. Water bath. A detailed description of the subject matter of the contract is enclosed as appendix no. 3 to the SWZ - description of the subject matter of the contract.1Under pain of invalidity, the Contracting Authority demands that the following means of proof be submitted with the tender in electronic form to confirm that the supplies offered meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to check quality, confirming that the products supplied conform to certain harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows the submission of the documents referred to in item 2) in English.2. Thermocycler. A detailed description of the subject matter of the contract is enclosed as Attachment 3 to the SWZ - Description of the subject matter of the contract.1The Contracting Authority demands that the following proofs of quality be submitted together with the tender under pain of invalidity, in an electronic form, to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the supplied products meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part No. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows the submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or if the submitted evidence is incomplete, the Contracting Authority shall call for its submission or supplementation within the prescribed time limit. Water bath with shaking. A detailed description of the subject matter of the contract is enclosed as appendix no. 3 to the SWZ - description of the subject matter of the contract.1Under pain of invalidity, the Contracting Authority demands that the following means of proof be submitted with the tender in electronic form to confirm that the supplies offered meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to check quality, confirming that the products supplied conform to certain harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part No. and position of the offered subject matter of the contract).NOTE: The Contracting Authority accepts submission of the documents mentioned in item 2) in English.2. Centrifuge with cooling. Detailed description of the subject matter of the contract is provided in Attachment No. 3 to SWZ - Description of the subject matter of the contract.1The Contracting Authority demands submitting, together with the tender, under pain of invalidity, in an electronic form, the following means of evidence to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate issued by an entity authorised to control quality, confirming that the supplied products meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows submission of the documents referred to in item 2) in English.2. Electroporator. A detailed description of the subject matter of the contract is attached as appendix no. 3 to the SWZ - description of the subject matter of the contract.1The Contracting Authority demands that the following means of proof be submitted together with the tender under pain of invalidity in electronic form to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the supplied products meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority accepts submission of the documents referred to in item 2) in English.2. Vacuum concentrator. A detailed description of the subject matter of the contract is attached as appendix no. 3 to the SWZ - Description of the subject matter of the contract.1Under pain of invalidity, the Contracting Authority demands that the following means of proof be submitted with the tender in electronic form to confirm that the supplies offered meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the products supplied conform to certain harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part no. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows the submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or the submitted evidence is incomplete, the Contracting Authority shall call for its submission or supplementation within the prescribed time limit. System for real-time PCR analysis with equipment. A detailed description of the subject matter of the contract is attached as appendix 3 to the SWZ - Description of the subject matter of the contract.1The Contracting Authority demands that the following means of proof be submitted with the tender under pain of invalidity, in electronic form, to confirm that the offered supplies meet the requirements specified by the Contracting Authority:1) A certificate from an entity authorised to control quality, confirming that the supplied products meet the specified harmonised standards or technical specifications, in accordance with the Act of 20 May 2010 on medical devices (i.e. Journal of Laws of 2019, item 175, as amended), i.e.:a) a document confirming the notification of the device to the President of the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products, hereinafter referred to as the President of the Office, or a document3 / 14 confirming the notification to the President of the Office of the introduction into the territory of the Republic of Poland of a device intended for use in that territory;b) a certificate of conformity in cases defined in the law on medical devices; c) a declaration of conformity, confirming that the medical device complies with the essential requirements; d) if the item described in the Terms of Reference is not classified as a medical device, the Contracting Authority requires submission of an appropriate statement confirming the Contracting Authority's requirements.NOTE:- If a document confirming notification to the President of the Office is issued for a medical device, then the contractor should only submit the document referred to in paragraph 1.a) of this section. If the document referred to in paragraph 1.a) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.b) of this chapter.- If the document referred to in paragraph 1.b) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.c) of this chapter.- If the document referred to in paragraph 1.c) is not issued for a medical device, then the contractor shall submit the document referred to in paragraph 1.d) of this chapter. - 2) Information materials containing a description of the offered subject matter of the contract (prospectus, catalogue, card, technical data form, etc.), confirming the requirements included in Enclosure No. 3 to the SWZ (indicating the required parameters, part No. and position of the offered subject matter of the contract).NOTE: The Contracting Authority allows submission of the documents referred to in item 2) in English.2. If the Economic Operator fails to submit the said evidence or if the submitted evidence is incomplete, the Contracting Authority shall call for its submission or completion within the prescribed time limit.

Opportunity closing date
20 September 2021
Value of contract
to be confirmed

About the buyer

Address
Instytut Matki i Dziecka ul. Kasprzaka 17A Warszawa 01-211 Poland
Contact
witold.sarnowski@imid.med.pl

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