GUDIDData
eudamed_udi Primary ID: 06942013202368

Extra Mini Kit (UDI 06942013202368)

Manufactured by Hubei V-Medical Products Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Extra Mini Kit - Primary ID 06942013202368

Device Regulatory Overview

The Extra Mini Kit (Model/Catalog Number: 21049) is a medical device manufactured by Hubei V-Medical Products Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification V9012 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
21049
Product Code / EMDN
V9012
Device Name
First Aid Kit
Database Sync Date
2026-08-09 16:30:22

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 Extra Mini Kit?

The registered manufacturer of record for Extra Mini Kit is Hubei V-Medical Products Co.,Ltd..

What is the Primary UDI-DI identifier for Extra Mini Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06942013202368.

What classification code is assigned to this device?

This device is registered under product classification code V9012.

Programmatic Export

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

JSON API Endpoint