Catalogue number LIO Keeler, listed by Lumenis, Ltd., Israel, under Instrument, Vitreous Aspiration And Cutting, Ac-Powered. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for LIO Keeler | Listed by | Lumenis, Ltd., Israel |
| FDA product code | HQE |
| Device type | Instrument, Vitreous Aspiration And Cutting, Ac-Powered |
| Device class | Class 2 |
| Regulation | 21 CFR 886.4150 |
| Establishment | Specification developer, Manufacturer |
| Record published | 2016-08-31 |
| Record revised | 2023-08-01 (version 5) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Prescription | Prescription only |
| Label carries | manufacturing date, serial number |
| Distribution end date | 2023-07-31 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.