GUDIDData
eudamed_udi Primary ID: 06973685040927

Unspecified Brand (UDI 06973685040927)

Manufactured by FOMED INDUSTRIES INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06973685040927

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 150 mm×200 m) is a medical device manufactured by FOMED INDUSTRIES INC.. This product is indexed under FDA Product Code / Category Classification S01020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
150 mm×200 m
Product Code / EMDN
S01020101
Device Name
Flat reels
Database Sync Date
2026-08-09 16:48:09

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is FOMED INDUSTRIES INC..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973685040927.

What classification code is assigned to this device?

This device is registered under product classification code S01020101.

Programmatic Export

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

JSON API Endpoint