GUDIDData
eudamed_udi Primary ID: 06976714790114

Unspecified Brand (UDI 06976714790114)

Manufactured by Linfen Houma Economic Development Zone Yongxing 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 06976714790114

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 20kg) is a medical device manufactured by Linfen Houma Economic Development Zone Yongxing Medical Device Co.,Ltd. This product is indexed under FDA Product Code / Category Classification M04040201,M04040202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
20kg
Product Code / EMDN
M04040201,M04040202
Device Name
Alginate Impression
Database Sync Date
2026-08-09 17:28:43

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 Linfen Houma Economic Development Zone Yongxing 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 06976714790114.

What classification code is assigned to this device?

This device is registered under product classification code M04040201,M04040202.

Similar Classification Devices (M04040201,M04040202)

Other Devices by Linfen Houma Economic Development Zone Yongxing Medical Device Co.,Ltd

Programmatic Export

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

JSON API Endpoint