GUDIDData
eudamed_udi Primary ID: 04582667989301

EYEVAN (UDI 04582667989301)

Manufactured by EYEVAN Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EYEVAN - Primary ID 04582667989301

Device Regulatory Overview

The EYEVAN (Model/Catalog Number: SADLER 47 MOR) is a medical device manufactured by EYEVAN Inc.. This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SADLER 47 MOR
Product Code / EMDN
Q02100202
Device Name
Plastic spectacle frames without lenses
Database Sync Date
2026-08-09 16:29:43

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 EYEVAN?

The registered manufacturer of record for EYEVAN is EYEVAN Inc..

What is the Primary UDI-DI identifier for EYEVAN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04582667989301.

What classification code is assigned to this device?

This device is registered under product classification code Q02100202.

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