OPHTHALMIC FEMTOSECOND LASER
This device is manufactured by WAVELIGHT GMBH, WAVELIGHT GMGH.
The following problems were reported about this device:
| Year | Description | Events/year | Type |
|---|---|---|---|
| 2024 | Visual Impairment | 1 | Patient |
| 2024 | Insufficient Information | 21 | Patient |
| 2024 | Inflammation | 1 | Patient |
| 2024 | Corneal Perforation | 1 | Patient |
| 2024 | Appropriate Term / Code Not Available | 17 | Patient |
| 2024 | Suction Problem | 2 | Device |
| 2024 | Failure to Align | 28 | Device |
| 2024 | Decrease in Suction | 2 | Device |
| 2024 | Adverse Event Without Identified Device or Use Problem | 2 | Device |
| 2023 | Visual Impairment | 1 | Patient |
| 2023 | Unspecified Eye / Vision Problem | 1 | Patient |
| 2023 | Keratitis | 7 | Patient |
| 2023 | Insufficient Information | 4 | Patient |
| 2023 | Corneal Perforation | 1 | Patient |
| 2023 | Appropriate Term / Code Not Available | 19 | Patient |
| 2023 | Suction Problem | 1 | Device |
| 2023 | Failure to Align | 28 | Device |
| 2023 | Decrease in Suction | 1 | Device |
| 2023 | Appropriate Term/Code Not Available | 1 | Device |
| 2023 | Adverse Event Without Identified Device or Use Problem | 9 | Device |
| 2022 | Insufficient Information | 1 | Patient |
| 2022 | Appropriate Term / Code Not Available | 1 | Patient |
| 2022 | Suction Problem | 1 | Device |
| 2022 | Failure to Align | 11 | Device |
| 2022 | Decrease in Suction | 1 | Device |
| 2022 | Adverse Event Without Identified Device or Use Problem | 3 | Device |
| 2020 | Suction Problem | 1 | Device |
| 2020 | Device Operates Differently Than Expected | 1 | Device |