GUDIDData
eudamed_udi Primary ID: 08809306768292

VIVA RF electrode (UDI 08809306768292)

Manufactured by STARmed Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIVA RF electrode - Primary ID 08809306768292

Device Regulatory Overview

The VIVA RF electrode (Model/Catalog Number: 15-25V05-30X_V2) is a medical device manufactured by STARmed Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K0201010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
15-25V05-30X_V2
Product Code / EMDN
K0201010301
Device Name
VIVA RF electrode
Database Sync Date
2026-08-09 16:29:26

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 VIVA RF electrode?

The registered manufacturer of record for VIVA RF electrode is STARmed Co., Ltd..

What is the Primary UDI-DI identifier for VIVA RF electrode?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809306768292.

What classification code is assigned to this device?

This device is registered under product classification code K0201010301.

Programmatic Export

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

JSON API Endpoint