Catalogue number 3020-P-7046, listed by Keeler Ltd., United Kingdom, under Camera, Ophthalmic, Ac-Powered. 3 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (1), Shanghai (1), Chongqing (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Keeler Kapture Lite to View Plus Upgrade | Listed by | Keeler Ltd., United Kingdom |
| FDA product code | HKI |
| Device type | Camera, Ophthalmic, Ac-Powered |
| Device class | Class 2 |
| Regulation | 21 CFR 886.1120 |
| Establishment | Contract manufacturer, Specification developer, Manufacturer |
| Record published | 2016-08-26 |
| Record revised | 2022-12-20 (version 6) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Label carries | manufacturing date, serial number |
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.