Salient Characteristics.pdf
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- Attached to
- Brand Name or Equal Comprehensive Optical Biometer Federal contract opportunity
- Solicitation number
- 36C24425Q0487
About this file
This document is a Salient Characteristics file for the Zeiss IOL Master 700, specifying detailed technical requirements for a comprehensive optical biometer for the Philadelphia VA Medical Center. The device must be fully compatible with the Carl Zeiss ecosystem, specifically the ZEISS FORUM data management system, and provide advanced ophthalmic measurement capabilities including contactless Swept Source OCT Biometry, corneal topography, and integrated surgical planning features.
Key technical requirements include completing full biometry measurements in under 1 minute, providing comprehensive cornea-to-retina scans, automated data transfer, DICOM compatibility, and seamless integration with existing medical record systems. The device must have an ergonomic design with adjustable patient positioning features, be compatible with U.S. electrical outlets, and hold FDA approval for ophthalmic biometry while complying with ISO medical device standards. The solicitation is part of the Department of Veterans Affairs Veterans Health Administration's procurement process, with quotes due by 4:00 PM EST on 5/12/2025, to be submitted via email to joanne.skaff@va.gov.
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Other files for this federal contract opportunity
| File | Type | Posted |
|---|---|---|
| STATEMENT OF NEED.pdf | ||
| 36C24425Q0487 LineItems.xlsx | XLSX spreadsheet | |
| 36C24425Q0487_1.pdf |
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Text version
Brand Name Item: Zeiss IOL Master 700 (SALIENT CHARACTERISTICS)
ALL ITEMS MUST BE COMPATIBLE WITH THE CARL ZEISS ECOSYSTEM, SPECIFICALLY THE ZEISS FORUM.
1. Measurement technology and accuracy:
a. Contactless Swept Source OCT Biometry
i. Must be capable of providing axial length, keratometry, and central anterior chamber depth measurements.
b. Corneal topography
i. Must be capable of providing posterior and anterior corneal topography to enhance IOL calculations.
2. IOL calculation and surgical planning capabilities:
a. Must include integrated Barret Suite.
b. Must include markless Tori IOL alignment.
c. Must be capable of reducing the risk of refractive surprise.
3. Workflow efficiency and data management:
a. Automated biometry measurement:
i. Must be capable of completing full biometry in under 1 minute for both eyes.
b. Full length OCT image capture
i. Must be capable of providing a comprehensive cornea-to-retina scan to detect potential measurement errors
c. Automated data transfer:
i. Must be capable of seamlessly integrating with ophthalmic data management systems already in place to eliminate manual data entry errors. The data management system in place is the ZEISS FORUM.
ii. Must be capable of transferring data via ZEISS FORUM into the biometry unit and vice versa.
d. DICOM compatibility:
i. Must be DICOM-compliant to interface with electronic medical record systems.
4. Physical and Operational Requirements
a. Must have a compact and ergonomical design.
b. Must include patient positioning features.
i. Adjustable chin rest.
ii. Head support for stable measurements.
c. Must be compatible with standard U.S. electrical outlets.
d. Must be FDA-approved for use in ophthalmic biometry and comply with ISO standards for medical devices.
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