FDA UDI In Commercial Distribution 🇺🇸 United States

AUTO REFRACTOMETER

DI: 04987669101469 · Model: AR-F · NIDEK CO.,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AUTO REFRACTOMETER
Primary DI
04987669101469
Version / Model
AR-F
Company Name
NIDEK CO.,LTD.
Labeler DUNS
690635461
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-22
Public Version
3
Public Version Date
2020-12-21
Public Version Status
Update
Public Device Record Key
7b6312f2-a0a9-4753-bb57-3b77a0a92b3e

Device Description

The AUTO REFRACTOMETER AR-F is a medical device which measures objective refractive errors of the patient’s eye. This device also offers retroillumination mode for observing the condition of the ocular media, and measures the amplitude of accommodation.

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 04987669101469

Customer Contacts