Place of Origin:
China
Brand Name:
SYSEYE
Certification:
FDA
Model Number:
RetiCam 3100
Contact Us
ophthalmic fundus camera SLR camera one-key click 135° wide field
Digital Fundus Camera RetiCam 3100 can be used to capture the anterior and posterior eye images. It has a field of view of 50 degrees for fundus imaging.Digital Fundus Camera Reticam 3100 is a highly recognized and popular automatic fundus imaging system around the world. Through dual camera imaging, image control and feature recognition, eye XYZ 3D automatic positioning is realized. Through CCD imaging feedback, the exposure is measured, and the exposure intensity is automatically and accurately determined, without the need for a doctor's complex operation. By controlling the focusing step length according to the image resolution, the image definition can be automatically adjusted to obtain a clear and accurate fundus image and help doctors make accurate judgments for patients.
| Field of view | 50° |
| Field of view tolerance | ±7% |
| Resolution | |
| Center of view | ≥60 lp/mm |
| Field of view center (r/2) | ≥40 lp/mm |
| At the edge of the field of view (r) | ≥25 lp/mm |
| Magnification | 1.3 times |
| Required pupil diameter | 4.0 mm or more (3.3 mm or more when using the small pupil shooting function) |
| Working distance | 35 mm |
| Focus adjustment range | ±25D |
| Shooting light | Auto: with shooting mode |
| Manual: can be set manually | |
| light source | |
| Illumination light | Infrared led |
| Shooting light | Xenon lights |
| reflected light | |
| Scattered light | |
| camera | Digital camera |
| Fixing light | Internal fixing light (LED) |
| External fixation light | |
| Moving range | |
| Stage | 90 mm left and right, 35 mm front and rear |
| Main unit moves vertically | 30 mm |
| Chin-rest tray movement range | 60 mm |
| Rated power supply | AC 100V~240V,50/60Hz |
| size | 380 mm(L)x 550 mm(W)x 475 mm(H) |
| weight | About 26.5kg |
| When in maximum light intensity/hole bar state | |
| Spectral wavelength | 305 nm~1100 nm |
| Equipment classification | ||
| Electric shock protection | Class I device | |
|
Degree of electric shock protection |
Type B |
|
|
Water-proof protection |
IPX0 |
|
|
Safety level for use in flammable anesthetic gases, oxygen or nitrous oxide mixed with air |
Not applicable |
|
| Standards | ||
|
GB 9706.1-2007 IEC 60601-1:1998 + A1:1991 + A2: 1995 |
Medical electrical equipment - Part 1: General requirements for safety | |
|
IEC 60601-1:2005 |
Medical electrical equipment - Part 1: General requirements for basic safety and practical performance |
|
|
IEC 60601-1-1:2000 |
Medical electrical equipment - Part 1-1: General requirements for safety - Parallel standard: Safety requirements for medical electrical systems |
|
|
IEC 60601-1-2:2001 + A1:2004 |
Medical electrical equipment - Part 1-2: General requirements for safety - Parallel standard: Electromagnetic compatibility - Requirements and testing |
|
|
IEC 60601-1-2:2007 |
Medical electrical equipment – Part 1-2: Basic safety and General requirements for practical performance – side-by-side standards: electromagnetic compatibility – requirements and testing |
|
| IEC 60601-1-4:1996 + A1:1999 |
Medical Electrical Equipment - Part 1-4: Safety General Seeking – Parallel Standard: Programmable Medical Electrical System |
|
IEC 60601-1-6:2010 |
Medical electrical equipment - Part 1-6: General requirements for basic safety and practical performance - Parallel standard: Availability |
|
ISO 14971:2007 |
Medical Devices – Risk Management for Medical Devices |
|
ISO 15004-1:2006 |
Ophthalmic instruments - Test methods for basic requirements - Part 1: General requirements for all ophthalmic instruments |
|
ISO 15004-2:2007 |
Ophthalmic instruments - Test methods for basic requirements - Part 2: |
|
ISO 10940:2009 |
Ophthalmic Instruments - Fundus Camera |
|
ISO 10993-1:2009 ISO 10993-5:2009 ISO 10993-10:2010 |
Biological evaluation of medical devices |
|
IEC 62304:2006 |
Medical Device Software - Software Lifecycle Process |
|
IEC 62366:2007 |
Medical Devices – Usability Engineering for Medical Devices |
|
GB/T 191-2008 |
Packaging storage and transportation icon |
|
GB 4824-2013 |
Industrial, scientific and medical (ism) radio frequency equipment disturbance characteristics limits and methods of measurement |
|
GB/T 14710-2009 |
Medical electrical environment requirements and test methods |
|
GB/T 16886.1-2011 |
Medical Device Biology Evaluation - Part 1: Evaluation and Testing in Risk Management Process |
|
GB/T 16886.5-2003 |
Biological evaluation of medical devices - Part 5: In vitro cytotoxicity test |
|
GB/T 16886.10-2005 |
Biological evaluation of medical devices - Part 10: Stimulation and delayed hypersensitivity test |
| GB/T 5702-2003 | Light source color evaluation method |
|
YY 0634-2008 |
Ophthalmic instrument fundus camera |
|
YY 0505-2012 |
Medical electrical equipment - Part 1-2: General requirements for safety - Parallel standard: Electromagnetic compatibility - Requirements and testing |
Send your inquiry directly to us
