| Primary Device ID | 10380657900197 |
| NIH Device Record Key | 90bc0ff9-a495-485e-9c83-a32b0559e039 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Alcon, Kelman, TurboSonics, ABS, MicroTip |
| Version Model Number | 8065790019 |
| Company DUNS | 008018525 |
| Company Name | Alcon Laboratories, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com | |
| Phone | +1(800)862-5266 |
| web.masterus@alcon.com |
| Angle | 0 degree |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Outer Diameter | 0.9 Millimeter |
| Angle | 0 degree |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00380657900190 [Primary] |
| GS1 | 10380657900197 [Package] Contains: 00380657900190 Package: Box [6 Units] In Commercial Distribution |
| HQC | Unit, phacofragmentation |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-24 |
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| 00380658435615 - Clareon PanOptix Pro | 2025-04-04 CLAREON PANOPTIX PRO TORICUV |
| 00380658435622 - Clareon PanOptix Pro | 2025-04-04 CLAREON PANOPTIX PRO TORICUV |
| 00380658435639 - Clareon PanOptix Pro | 2025-04-04 CLAREON PANOPTIX PRO TORICUV |
| 00380658435646 - Clareon PanOptix Pro | 2025-04-04 CLAREON PANOPTIX PRO TORICUV |
| 00380658435653 - Clareon PanOptix Pro | 2025-04-04 CLAREON PANOPTIX PRO TORICUV |
| 00380658435660 - Clareon PanOptix Pro | 2025-04-04 CLAREON PANOPTIX PRO TORICUV |