gudid Primary ID: 0395-2572:L48

FOGG SYSTEM COMPANY, INC. (UDI 0395-2572:L48)

Manufactured by Fogg System Company, Inc.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FOGG SYSTEM COMPANY, INC. (Model/Catalog Number: 0395-2572:L48) is a medical device manufactured by Fogg System Company, Inc.. This product is indexed under FDA Product Code / Category Classification DSA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 0395-2572:L48
Product Code / EMDN: DSA
Device Name: 0395-2572 Interface Cable
Database Sync Date: 2026-08-09 09:27:12

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 FOGG SYSTEM COMPANY, INC.?

The registered manufacturer of record for FOGG SYSTEM COMPANY, INC. is Fogg System Company, Inc..

What is the Primary UDI-DI identifier for FOGG SYSTEM COMPANY, INC.?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 0395-2572:L48.

What classification code is assigned to this device?

This device is registered under product classification code DSA.

Similar Classification Devices (DSA)

Other Devices by Fogg System Company, Inc.

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