eudamed_udi Primary ID: 06977730470141

Acetate optical frames (UDI 06977730470141)

Manufactured by Wenzhou XinRui Glasses Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Acetate optical frames (Model/Catalog Number: ID Tokyo GLF5908) is a medical device manufactured by Wenzhou XinRui Glasses Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ID Tokyo GLF5908
Product Code / EMDN: K01010103
Device Name: GLF5907/GLF5908/GLF5909/GLF5910
Database Sync Date: 2026-08-09 17:49:45

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 Acetate optical frames?

The registered manufacturer of record for Acetate optical frames is Wenzhou XinRui Glasses Co., Ltd..

What is the Primary UDI-DI identifier for Acetate optical frames?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06977730470141.

What classification code is assigned to this device?

This device is registered under product classification code K01010103.

Similar Classification Devices (K01010103)

Other Devices by Wenzhou XinRui Glasses Co., Ltd.

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