GUDIDData
gudid Primary ID: VN-150

GTK (UDI VN-150)

Manufactured by Guangzhou T.K Medical Instrument Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GTK - Primary ID VN-150

Device Regulatory Overview

The GTK (Model/Catalog Number: VN-150) is a medical device manufactured by Guangzhou T.K Medical Instrument Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification HIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VN-150
Product Code / EMDN
HIF
Device Name
Database Sync Date
2026-08-09 09:04:56

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 GTK?

The registered manufacturer of record for GTK is Guangzhou T.K Medical Instrument Co.,Ltd..

What is the Primary UDI-DI identifier for GTK?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VN-150.

What classification code is assigned to this device?

This device is registered under product classification code HIF.

Programmatic Export

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

JSON API Endpoint