GUDIDData
eudamed_udi Primary ID: 06978468040934

RED SWISS (UDI 06978468040934)

Manufactured by Superb Vision International Trading (Hangzhou) Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RED SWISS - Primary ID 06978468040934

Device Regulatory Overview

The RED SWISS (Model/Catalog Number: RO8324AU C4) is a medical device manufactured by Superb Vision International Trading (Hangzhou) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RO8324AU C4
Product Code / EMDN
Q02100202
Device Name
SPECTACLE FRAMES
Database Sync Date
2026-08-09 16:29:10

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 RED SWISS?

The registered manufacturer of record for RED SWISS is Superb Vision International Trading (Hangzhou) Co.,Ltd..

What is the Primary UDI-DI identifier for RED SWISS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978468040934.

What classification code is assigned to this device?

This device is registered under product classification code Q02100202.

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