36C24818Q9807-002.pdf

Attachment B

RFQ: 36C24818Q9807

Line Item Description Qty Unit

Unit Price

Total Price

Archive and Viewer Package Must Include: 1 Archive, 3 Viewer and 3 DICOM CZM Instrument Connections EA 1

0002 Viewer License, Floating EA 1

0003 Viewer License, Volume Pack (10x) EA 1

0004 Glaucoma Workplace EA 1

0005 Glaucoma Workplace User License EA 1

Glaucoma Workplace User Volume Pack (10x) EA 1

0007 Retina Workplace EA 1

0008 Retina Workplace User License EA 1

Retina Workplace User Volume Pack (10x) EA 1

Bi-Directional DICOM Interface License to CZM Instrument EA 3

Interface License to 3rd party DICOM Instruments. EA 1

Upgrade to Cirrus Instrument Review Software with Remove Installation. EA 1

0013 Onsite Installation and User Training EA 1

0014 Connectivity Service Plan EA 1

Enterprise Architecture Design – Must be completed on before the 30th of October, 2018 JB 1

Training - Must be completed on before the 30th of October, 2018 JB 1

Total Cost

Salient Characteristics:

• Image and Data Management System must be FDA 510k approved and listed as a Medical Device.

Attachment B

RFQ: 36C24818Q9807

• Image and Data Management System must provide “Post Processing Analysis, Dynamic Review/Manipulation of RAW data” functionality for ZEISS Cirrus HD-OCT.

• Image and Data Management System must be able to download all past RAW data from one or more ZEISS Field Analyzers, ZEISS Cirrus HD-OCT’s, ZEISS Visucam Fundus Camera and ZEISS FF450/Visupac Fundus Cameras acquired within the main clinic and all satellite clinics upon installation of the Image and Data Management System.

• Image and Data Management System must support DICOM standards and Work-List functionality in order to create and send patient demographics to a specific or all instruments via a DICOM work-list within the eye clinic’s network.

• Image and Data Management System must connect to any brand of non- DICOM diagnostic instrument with export capabilities, and convert the diagnostic test results into a DICOM compatible file containing all patient demographical information, UID’s, Accession number, Device name and type, laterality and other key pieces of data with the least amount of user interaction.

• Image and Data Management System must not require the use of an external PC or import computer for a DICOM compatible modality.

• Image and Data Management System must be able to display images in preformatted clinical display groupings for Glaucoma, Retina and Cataract cases.