GUDIDData
eudamed_udi Primary ID: 08809854025076

Unspecified Brand (UDI 08809854025076)

Manufactured by MegaGen Implant Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08809854025076

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: STHA404MN) is a medical device manufactured by MegaGen Implant Co., Ltd.. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
STHA404MN
Product Code / EMDN
P01020101
Device Name
Healing Abutment
Database Sync Date
2026-08-09 16:28:45

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 MegaGen Implant 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 08809854025076.

What classification code is assigned to this device?

This device is registered under product classification code P01020101.

Programmatic Export

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

JSON API Endpoint