eudamed_udi Primary ID: 03701411813599

Europe C1 (UDI 03701411813599)

Manufactured by Paname

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Europe C1 (Model/Catalog Number: EUROPE C1) is a medical device manufactured by Paname. This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: EUROPE C1
Product Code / EMDN: Q02100202
Device Name: Spectacle frames without lenses — Full rim, Acetate front, Acetate temples
Database Sync Date: 2026-08-09 16:28:54

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 Europe C1?

The registered manufacturer of record for Europe C1 is Paname.

What is the Primary UDI-DI identifier for Europe C1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701411813599.

What classification code is assigned to this device?

This device is registered under product classification code Q02100202.

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