FDA UDI In Commercial Distribution 🇺🇸 United States

AUTO REF/KERATOMETER

DI: 06971821402127 · Model: ARK-910 · Ningbo Ming Sing Optical R & D Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AUTO REF/KERATOMETER
Primary DI
06971821402127
Version / Model
ARK-910
Company Name
Ningbo Ming Sing Optical R & D Co., Ltd.
Labeler DUNS
654386890
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-03
Public Version
1
Public Version Date
2021-11-11
Public Version Status
New
Public Device Record Key
8200e49a-759e-4049-bfd2-aa96df0f71f2

Device Description

Structure: composed of optical imaging system, control system and display. Working principle: AUTO REF/KERATOMETER is to use infrared fundus reflex phase method, by launching a specific wavelength beam of infrared light, through the examiner cornea, lens and so on, finally projected onto the retina eyeball, then reflected back to the corresponding optical system, absorb the image by image sensor, after image processing, signal processing, calculate the ball lens diopter, axial column lens dioptre, column mirror, An instrument used to determine the refractive state of the human eye. AUTO REF/KERATOMETER can move in X axis, Y axis and Z axis at the same time, with 3D automatic eye tracking function.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HKO Refractometer, Ophthalmic

GMDN Terms

Code Name
36386 Automated ophthalmic refractometer

Identifiers

Type ID
Primary 06971821402127

Customer Contacts