eudamed_udi Primary ID: 06976752175201

Optical frame (UDI 06976752175201)

Manufactured by DANYANG SUNTEX IMP. & EXP. CO., LTD.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Optical frame (Model/Catalog Number: Niccolo Giovanni NG52811 C3) is a medical device manufactured by DANYANG SUNTEX IMP. & EXP. CO., LTD.. This product is indexed under FDA Product Code / Category Classification Q02100203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Niccolo Giovanni NG52811 C3
Product Code / EMDN: Q02100203
Device Name: optical frame
Database Sync Date: 2026-08-09 16:28:48

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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Frequently Asked Questions

Who is the primary manufacturer of Optical frame?

The registered manufacturer of record for Optical frame is DANYANG SUNTEX IMP. & EXP. CO., LTD..

What is the Primary UDI-DI identifier for Optical frame?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976752175201.

What classification code is assigned to this device?

This device is registered under product classification code Q02100203.

Similar Classification Devices (Q02100203)

Other Devices by DANYANG SUNTEX IMP. & EXP. CO., LTD.

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