Operator's Manual
Table Of Contents
- Table of Contents
- 1 — Introduction
- 2 — Warnings, Cautions, and Other Residual Risks
- 3 — System Components
- 4 — Surgery Start Up
- 5 — Surgeon Settings
- 6 — Program Settings
- 7 — System Configuration
- Setting the Maximum IV Pole Height
- Testing the IV Pole
- Event Log
- Wireless Foot Pedal Setup
- VERITAS Remote Control Setup
- System Versions
- System Self Test
- Language Selection
- Surgical Media Center (SMC) (Optional)
- Set System Date and Time
- Set Units of Measure for Vacuum
- Service Interval
- Import/Export Database
- Backup All
- Print to File
- Restore Database
- Restore All
- Delete a Backup Database
- 8 — Symbol Definitions
- 9 — Care and Cleaning
- 10 — Error Messages, Troubleshooting, and Diagnostics
- 11 — Warranty and Maintenance
- 12 — Specifications
- Physical Specifications
- Environmental Specifications
- Electrical Specifications
- Electromagnetic Compatibility
- RF Wireless Technology
- Bluetooth Characteristics
- Phacoemulsification Specifications
- Irrigation and Aspiration Specifications
- Vitrectomy Specifications
- Diathermy Specifications
- Diathermy Power Graphs
- Diathermy Power versus Load Impedance
- Phaco Power Graphs
- Phaco Tip Velocity
- Bottle Height Pressure
- 13 — Accessories and Parts Reordering
- Index
Intended Use / Indications Z370584 Rev. C
1-4
Introduction
NOTE: Provides background information to clarify a particular step or procedure.
Intended Use / Indications
The VERITAS Vision System is a modular ophthalmic microsurgical system that facilitates
anterior segment (cataract) surgery. The modular design allows the users to configure the
system to meet their surgical requirements.
Contraindications
Any pre-existing patient condition/s that the health care provider determines to be a
contraindication to cataract surgery.
Undesirable Side Effects
Complications that may be associated with the VERITAS Vision System include
• corneal burn
• infection/inflammation
• corneal edema
• broken capsule
Intended Patient
Adult patients with cataracts or adult patients undergoing anterior segment ophthalmic
surgery (e.g., removal of the crystalline lens).
NOTE: Pregnant or nursing women were not included in the clinical trial(s) conducted.
Intended User
The JJSV Phacoemulsification System is intended for use by an ophthalmologist and support
staff operating under the direction of the surgeon.
IMPORTANT:
Identifies instructions important to the proper operation of the device.