gudid
Primary ID: iRef
MOPTIM (UDI iRef)
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 iRef
Device Regulatory Overview
The MOPTIM (Model/Catalog Number: iRef) is a medical device manufactured by Shenzhen CERTAINN Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification HKO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- iRef
- Product Code / EMDN
- HKO
- Device Name
- The manual refractometer is composed of a lens and a removable eye chart. The testee is required to move the position of the eye chart after resetting to make the visual target become clearer from blur. Once the clearest position of the visual target is determined, the testees estimated refractive error can be read from the display screen of the instrument.
- Database Sync Date
- 2026-08-09 09:06:41
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 iRef.
What classification code is assigned to this device?
This device is registered under product classification code HKO.
Similar Classification Devices (HKO)
Other Devices by Shenzhen CERTAINN Technology Co., Ltd.
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