eudamed_udi Primary ID: 03701411802821

Ternes C1 (UDI 03701411802821)

Manufactured by Paname

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ternes C1 (Model/Catalog Number: TERNES C1) 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: TERNES C1
Product Code / EMDN: Q02100201
Device Name: Spectacle frames without lenses — Full rim, Metal front, Metal temples
Database Sync Date: 2026-08-09 16:29:19

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 Ternes C1?

The registered manufacturer of record for Ternes C1 is Paname.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701411802821.

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

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