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Med Autosight 900 Handheld Vision Screener, Portable Auto Ophthalmic Refractometer
US$2,100.00-3,640.00
1 Piece

Product profile

Customization

Available

Classification

Physiological Functions of Diagnosis and Monitoring Equipment

Type

ECG

Model NO.

MED-AutoSight 900

Certification

CE, FDA, ISO13485

Portable Auto Refractometer

Dimensions /200mm×80mm×270mm

Electrical Safety

Charger (Class I), Main Unit (Internally

Laser Safety

Laser (Class I), Wavelength 850nm,

Portable Auto Refractometer 1

Cylindrical(C) -3.00d~0.00d

Portable Auto Refractometer 2

Axis(a) 0°~180°

Portable Autorefractomer

Portable Auto-Refractor

Transport Package

Standard Packing for Export

Specification

CE

Trademark

Med Equipment

Origin

Guangzhou China

Production Capacity

1000/Month

Key features

FDA & CE Certified: Complies with CE, FDA, and ISO13485 standards for safety and quality.
Hartmann-Shack Technology: Uses wavefront sensor for accurate refractive error calculation.
Wide Measurement Range: Spherical: -9.00D to +8.00D; Cylindrical: -3.00D to 0.00D.
Portable Handheld Design: Compact dimensions 200x80x270mm for easy transport and use.
Dual Mode Operation: Supports Myopia Mode (-9.00D~+2.50D) and Normal Mode (-6.00D~+8.00D).
OEM/ODM Support: Customization services available for branding and specific needs.

Company profile

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 2010-06-18 CertifiedNearest Port: Guangzhou Port, Shenzhen PortAverage Response Time: ≤2.30h CertifiedTerms of Payment: LC, T/T, PayPal, etc.

AI-Powered supplier vetting

SummaryGuangzhou Med Equipment Limited is identified as a China-based limited company and factory-related medical and laboratory equipment supplier, established in 2015. The supplier presents a broad product range, including hospital, laboratory, surgical, dental, respiratory, and home-care equipment. Evidence indicates 10 production lines, a 1,660 m² manufacturing plant, 31–40 quality-control staff, and stated delivery within 15 workdays in both off-peak and peak periods. The supplier claims long-term warranties, technical support, after-sales service, and partnerships with more than 2,000 hospitals. However, certification information, detailed financial evidence, R&D strength, customization capability, and independently verifiable customer cases are not provided. There are also inconsistencies in the submitted company identity and operational profile, including differing legal names, employee counts, locations, and export-market descriptions, which warrant verification.
Supplier typeThe supplier is described as a factory, limited company, manufacturer, and one-stop medical and laboratory equipment supplier in China. Its stated offerings cover medical equipment, laboratory equipment, hospital infrastructure, consumables, veterinary equipment, and related solutions.
After-Sales capabilityThe supplier explicitly claims long-term warranties, technical support, comprehensive support, convenient purchasing, and timely after-sales service. These statements support a stated after-sales capability, although no service-level details or verification documents are provided.
Production capacityThe supplier reports 10 production lines, a 1,660 m² manufacturing plant, and 31–40 quality-control staff. It also states delivery within 15 workdays in both peak and off-peak seasons, providing explicit evidence of organized production and quality-control resources, although the reported factory and company details should be reconciled with other records.
Client casesThe supplier states that more than 2,000 hospitals have become business partners and that it supplies hospitals, clinics, research institutions, and universities. These are supplier-reported customer claims, but no named customers, project details, references, or independent verification are provided.

Product Q&A

Q:What is the measurement range for spherical error?
A:
The device supports Myopia Mode (-9.00D to +2.50D) and Normal Mode (-6.00D to +8.00D).
Q:Is this device suitable for children?
A:
Yes, it is used for preliminary determination of refractive error for both adults and children.
Q:What certifications does the AutoSight 900 have?
A:
It holds CE, FDA, and ISO13485 certifications.
Q:Can this device replace a professional eye exam?
A:
No, the result is for vision screening only and cannot replace a comprehensive eye exam.
Q:What is the working principle of the screener?
A:
It is based on Hartmann-Shack wavefront sensor technology to calculate diopter from reflected signals.

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