GUDIDData
gudid Primary ID: easyRef

MOPTIM (UDI easyRef)

Manufactured by Shenzhen CERTAINN Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MOPTIM - Primary ID easyRef

Device Regulatory Overview

The MOPTIM (Model/Catalog Number: easyRef) is a medical device manufactured by Shenzhen CERTAINN Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HKN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
easyRef
Product Code / EMDN
HKN
Device Name
The key technique used in the easyRef Handheld Auto Refractometer is based on principle of Hartmann wave-front sensing.Light is emitted from the light source system inside the device, and then focuses on the bottom of the eye through the spectroscope and exit port, then the light is reflected back to the device,and beam through lens system and received by CCD camera. It is possible to calculate the diopter of the human eye by detecting the offset between the relative calibration light and the spot array formed by the light spot of each sub-aperture.
Database Sync Date
2026-08-09 09:06:41

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of MOPTIM?

The registered manufacturer of record for MOPTIM is Shenzhen CERTAINN Technology Co., Ltd..

What is the Primary UDI-DI identifier for MOPTIM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is easyRef.

What classification code is assigned to this device?

This device is registered under product classification code HKN.

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