Catalogue number 000000-2194-446, listed by Carl Zeiss Vision Gmbh, Germany, under Stand, Instrument, Ac-Powered, Ophthalmic. 5 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Jiangsu (3), Beijing (1), Shaanxi (1). One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Visufit 1000 Platform | Listed by | Carl Zeiss Vision Gmbh, Germany |
| FDA product code | HMF |
| Device type | Stand, Instrument, Ac-Powered, Ophthalmic |
| Device class | Class 1 |
| Regulation | 21 CFR 886.1860 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer, Exporter |
| Premarket notification | Exempt |
| Record published | 2021-01-01 |
| Record revised | 2021-10-05 (version 2) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Label carries | manufacturing date, serial number |
| Storage | Handling environment humidity 30 to 85 % RH; Storage environment temperature -20 to 70 °C; Storage environment humidity 10 to 85 % RH; Handling environment temperature 10 to 40 °C; Handling environment atmospheric pressure up to 795 millibar; Storage environment atmospheric pressure 500 to 1060 millibar |
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.