eudamed_udi Primary ID: 03701411821617

ALBERTINE C7 (UDI 03701411821617)

Manufactured by Paname

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ALBERTINE C7 (Model/Catalog Number: Albertine C7) 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: Albertine C7
Product Code / EMDN: Q02100202
Device Name: Spectacle frames without lenses — Full rim, Acetate front, Acetate temples
Database Sync Date: 2026-08-09 16:46:16

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 ALBERTINE C7?

The registered manufacturer of record for ALBERTINE C7 is Paname.

What is the Primary UDI-DI identifier for ALBERTINE C7?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03701411821617.

What classification code is assigned to this device?

This device is registered under product classification code Q02100202.

Similar Classification Devices (Q02100202)

Other Devices by Paname

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