gudid Primary ID: S7000 Premium

FUSSEN (UDI S7000 Premium)

Manufactured by Fussen Technology Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FUSSEN (Model/Catalog Number: S7000 Premium) is a medical device manufactured by Fussen Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NOF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: S7000 Premium
Product Code / EMDN: NOF
Device Name
Database Sync Date: 2026-08-09 09:06:37

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 FUSSEN?

The registered manufacturer of record for FUSSEN is Fussen Technology Co., Ltd..

What is the Primary UDI-DI identifier for FUSSEN?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S7000 Premium.

What classification code is assigned to this device?

This device is registered under product classification code NOF.

Similar Classification Devices (NOF)

Other Devices by Fussen Technology Co., Ltd.

Programmatic Export

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

JSON API Endpoint