The OCULUS Easyfield® has been designed for combined use as a screening unit with all associated options for immediate follow-up examination of suspicious findings. The most common…
The OCULUS Easyfield® has been designed for combined use as a screening unit with all associated options for immediate follow-up examination of suspicious findings. The most common examination grids and strategies for the central visual field up to 30° can be accessed. The Easyfield® offers pre programmed combinations for often needed examination routines. For example: Screening 24-2, SPARK Quick, Macula. You can also combine your own routines and then save them as a program.
Who Else Makes It
Registered in Jiangsu.
Record
Regulatory record for Easyfield S | Listed by | Oculus Optikgeräte Gesellschaft mit beschränkter Haftung |
| FDA product code | HOO |
| Device type | Perimeter, Ac-Powered |
| Device class | Class 1 |
| Regulation | 21 CFR 886.1605 |
| Premarket notification | Exempt |
| Record published | 2016-09-01 |
| Record revised | 2018-03-29 (version 2) |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Prescription | Prescription only |
| Label carries | serial number |
| Storage | Storage environment temperature -10 to 55 °C; Storage environment humidity 10 to 95 % RH; Storage environment atmospheric pressure 70 to 106 KiloPascal; Handling environment temperature 10 to 40 °C; Handling environment humidity 30 to 75 % RH; Handling environment atmospheric pressure 70 to 106 KiloPascal |
| Sizes | Weight 4.6 kg; height 435 mm; depth 450 mm; width 275 mm |
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.