GUDIDData
eudamed_udi Primary ID: 04255908501975

M601 48◻20 143 C50 (UDI 04255908501975)

Manufactured by Alpha Collection

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for M601 48◻20 143 C50 - Primary ID 04255908501975

Device Regulatory Overview

The M601 48◻20 143 C50 (Model/Catalog Number: www.alphacollection.com) is a medical device manufactured by Alpha Collection. This product is indexed under FDA Product Code / Category Classification Q02100202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
www.alphacollection.com
Product Code / EMDN
Q02100202
Device Name
fullrim plastic spectacle frames
Database Sync Date
2026-08-09 16:30:18

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 M601 48◻20 143 C50?

The registered manufacturer of record for M601 48◻20 143 C50 is Alpha Collection.

What is the Primary UDI-DI identifier for M601 48◻20 143 C50?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04255908501975.

What classification code is assigned to this device?

This device is registered under product classification code Q02100202.

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