eudamed_udi Primary ID: 03701411814992

Henri C3 (UDI 03701411814992)

Manufactured by Paname

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Henri C3 (Model/Catalog Number: HENRI C3) is a medical device manufactured by Paname. This product is indexed under FDA Product Code / Category Classification Q02100201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HENRI C3
Product Code / EMDN: Q02100201
Device Name: Spectacle frames without lenses — Full rim, Metal front, Metal temples
Database Sync Date: 2026-08-09 16:29:55

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Henri C3?

The registered manufacturer of record for Henri C3 is Paname.

What is the Primary UDI-DI identifier for Henri C3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701411814992.

What classification code is assigned to this device?

This device is registered under product classification code Q02100201.

Similar Classification Devices (Q02100201)

Other Devices by Paname

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint