VERITAS^™ Vision System

INDICATIONS AND IMPORTANT SAFETY INFORMATION FOR THE VERITAS^™ Vision System

CAUTION
Federal law (USA) restricts this device to sale by or on the order of a physician

INDICATIONS FOR USE / INTENDED USES
The VERITAS Vision System is a modular ophthalmic microsurgical system that facilitates anterior segment (i.e., cataract) ophthalmic 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

PRECAUTIONS
Once you have set the system up and you have verified that all the functions are operating properly, you are almost ready to use your system. Read the following safety precautions carefully before using the system in surgery.
1. Do not use extension cords with your system.
2. Do not overload your electrical receptacle (outlet).
3. The instrument has ventilation openings at the rear of the console to allow ambient air intake and the release of heat generated during operation. Do not block the openings; as heat build-up can cause system failures which can result in a fire hazard.
4. Do not try to move the system cart on deep pile carpets or over objects on the floor, such as cables and power cords.
5. Take care not to trip over power and foot pedal cords.
6. Do not try to lift the system console.
7. Do not place the instrument on uneven or sloped surfaces.
8. Only use disposables, accessories, or other surgical instruments designed for this system. For optimum performance of the system and safety, use only parts recommended by JJSV.
9. Do not operate the system in a condensing environment (over 95% relative humidity). Take care to protect the instrument from fluid sprays or fluid buildup. To protect the patient from contaminated fluids or handpieces, use only: *sterile tubing packs *sterile irrigation fluid *sterile handpieces
10. Wrap the excess power cord neatly around the cord wrap on the back of the console.
11. Use caution when you use handpieces with sharp edges or pointed tips.
12. Always replace the tubing pack and the balanced salt solution bottle between cases.
13. Use extreme caution when you lower or raise the balanced salt solution bottle to decrease fluid flow or increase fluid flow, and fluid pressure.
14. If you do not properly prime the I/A tubing, errors can occur.
15. Care should be taken to avoid abrasion of tissues during phacoemulsification.
16. It is very important that the electrical connectors on the handpieces are completely dry before you attach the handpiece to the system receptacles.
17. The phaco handpiece is a very delicate instrument and you must handle the handpiece with EXTREME care.
18. The ultrasonic titanium phaco tip must never touch any solid material while in use.
19. Handpieces can be extremely hot immediately after sterilization. Use care and caution when handling.
20. Do not activate the phaco handpiece and vitrectomy cutter with the tip in the air. Exposure of the tip to air drastically reduces the useful life of the handpiece. If you introduce power to the phaco handpiece or vitrectomy cutter, the tip must be in a test chamber filled with balanced salt solution, in a container of balanced salt solution, or in the patient’s eye.
21. If there is damage to the cord or the plug, do not use the instrument. A damaged cable can cause an electric shock to the user or a fire hazard to the system. Call JJSV customer service to order a new cord.
22. Disconnect the power before you service the equipment.
23. Remove the power cord from the power outlet when the equipment is not in use.
24. Do not use the system in the presence of any of the following as a fire can result:
*flammable anesthetics
*other flammable gases
*flammable fluids
*flammable objects
*oxidizing agents
25. Ensure the patient does not have a cardiac pacemaker or other active implant as this unit might interfere with any cardiac pacemaker; therefore, obtain qualified advice prior to such use.
26. The patient must not come into contact with grounded metal parts or metal parts that have appreciable capacitance to ground. JJSV recommends the use of an antistatic mat for this purpose.
27. Use proper handling and disposal methods for biohazards when you dispose of the tubing pack, Mayo tray drape, and monitor drape.
28. Ensure the tubing pack drain bag does not over-fill. The maximum capacity of the bag is 600 cc. Do not obstruct the power outlet so you can readily remove the power cord.
29. To prevent the risk of fire or damage to the instrument, replace the fuses with the exact type and rating (check the voltage sticker on the back panel of the system to confirm your system voltage).
30. Not recommended for use in condensing environments. If exposed to a condensing environment, allow the system to equilibrate to typical operating room conditions prior to use. Only use the system within the stated relative humidity conditions.
31. You do not need to use a NEUTRAL ELECTRODE with this High Frequency (HF) Surgical Equipment.
32. Failure of this High Frequency (HF) Surgical Equipment could result in an unintended increase of output power.
33. Do not replace the foot pedal battery while in use with a patient.
34. Do not replace the remote control battery while in use with a patient.
35. Do not try to replace the batteries for the Advanced Control Pedal. Call your JJSV technical service representative to replace the batteries.
36. Sterility assurance is the responsibility of the user. You must sterilize all non-sterile accessories prior to use.
37. Prior to using any invasive portions of the handpiece assembly, examine under the microscope for any obvious damage, oxidation, or the presence of foreign material. You must note any questionable characteristics; use a backup handpiece for surgery. Use of contaminated or damaged system accessories can cause patient injury.
38. Do not have the handpiece tip in the eye of the patient when you prime and tune the handpiece.
39. Do not use non-JJSV approved products with the VERITAS Vision System, as this can affect overall system performance. JJSV cannot be responsible for system surgical performance if you use these products in surgery.
40. Use tips and sleeves that are designed to work together. Using improperly matching tip/sleeve combinations can result in insufficient fluid flow.
41. Do not use the sleeves beyond their useful life. Using sleeves beyond their useful life can result in insufficient fluid flow or debris in the eye.
42. Inspect batteries for damage before installation. Do not install damaged batteries. Installing damaged batteries could result in a fire.
43. Avoid balanced salt solution free flow conditions. Balanced salt solution free flow can result in a slip hazard.
44. The Advanced Infusion feature must only be used with bottles and is not to be used with bags. Using the Advanced Infusion feature with a bag may result in lower than expected irrigation pressure.
45. Do not use the ultrasonic tip beyond its specified useful life. Using the ultrasonic tip beyond its specified useful life may result in: *exfoliation of the tip leaving debris in the eye *reduced cutting capability, which may increase time required for surgery *insufficient flow of fluid
46. The VERITAS Swivel handpiece is an inseparable assembly. The user must not attempt to disassemble the swivel joint.
47. If the sterile packaging for a single-use accessory is damaged, notify JJSV. Do not use the accessory as sterility cannot be assured.
48. All tubing packs are single-use. Reusing a single-use device can cause bodily fluids from one patient to enter the eye of another patient. This can lead to medical conditions including: Toxic Anterior Segment Syndrome (TASS), Chemosis, Conjunctivitis Microbial, Endophthalmitis, Infectious Keratitis, Anterior Uveitis, and Keratoconjunctivitis.
49. Do not charge the Foot Pedal in the patient environment. Do not come in contact with patient when touching the device under charge.
50. When using Advanced Infusion, the effective bottle height cannot go below 30cm without re priming and selecting the Advanced Fluidics program.
51. This equipment/system is intended for use by healthcare professionals only. This equipment/system may cause radio interference or may disrupt the operation of nearby equipment. It may be necessary to take mitigation measures, such as re-orienting or relocating the VERITAS Vision System or shielding the location.
52. The VERITAS Vision System needs special precautions regarding electromagnetic compatibility (EMC) and needs to be installed and put into service according to the EMC information provided in this manual.
53. Portable and mobile RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the VERITAS Vision System, including cables specified by JJSV. Otherwise, degradation of the performance of this equipment could result.
54. The use of accessories, transducers and cables other than those specified by JJSV, may result in increased electromagnetic EMISSIONS or decreased electromagnetic IMMUNITY of the VERITAS Vision System.
55. The USB port should only be used for the data transfer purposes described in this manual. It should not be used to charge devices or connect peripheral devices. The VERITAS Vision System should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the VERITAS Vision System should be observed to verify normal operation in the configuration in which it will be used.
56. Do not replace the foot pedal battery when the pedal is attached to a power source.
57. Electrostatic Discharge (ESD) may disrupt the function and operation of the VERITAS Vision System and cause the system to go into a safe state and display an error message. If an error message occurs, follow the on-screen troubleshooting, or refer to the “Troubleshooting” section of the Operator’s manual. If the system requires restarting to resolve the error, be sure to remove the handpiece from the eye prior to shutting down the system.
58. The VERITAS Vision System may be interfered with by other equipment, even if that other equipment complies with regulatory emission requirements such as the International Special Committee on Radio Interference (CISPR).
59. Electromagnetic Disturbances from RFID readers are unlikely to affect the VERITAS Vision System; however antennas from RFID readers should be kept more than 2.5 cm (1 inch) from the system.
60. Inadvertent activation of functions that are intended for priming or tuning handpieces while the handpiece is in the eye can create a hazardous situation that could result in patient injury.
61. Danger of ignition of endogenous gases (e.g., cotton and gauze saturated with oxygen may be ignited by sparks produced during normal use of High Frequency (HF) Surgical Equipment).
62. Ensure the maximum capacity of the drain container is not exceeded as this could cause a hazardous situation to the patient.
63. The ophthalmic irrigation solution source shall be at or above the patient's eye level.
64. Never intentionally modify handpieces or tips (e.g., do not bend, cut, or engrave them) as they could break or malfunction.
65. Use caution when using clamps on a tubing set.
66. Use only recommended tubing set(s).
67. Do not touch an activated ultrasonic handpiece tip, as injuries could occur.
68. Use of accessories, transducers, and cables other than those provided with the VERITAS Vision System could cause increased electromagnetic emissions or decreased electromagnetic immunity of this equipment, resulting in improper operation.
69. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the VERITAS Vision System, including cables specified by JJSV. Otherwise, degradation of the performance of this equipment could result.

PP2023CT5086