GUDIDData
eudamed_udi Primary ID: 06941617119508

Unspecified Brand (UDI 06941617119508)

Manufactured by Henan Tuoren Medical Device Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06941617119508

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: FTTSC8040) is a medical device manufactured by Henan Tuoren Medical Device Co., Ltd. This product is indexed under FDA Product Code / Category Classification A0399 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
FTTSC8040
Product Code / EMDN
A0399
Device Name
Fluid Transfer Tubing Set
Database Sync Date
2026-08-09 16:49:00

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 Henan Tuoren Medical Device Co., Ltd.

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06941617119508.

What classification code is assigned to this device?

This device is registered under product classification code A0399.

Programmatic Export

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

JSON API Endpoint