GUDIDData
eudamed_udi Primary ID: 04719894384061

Reusable Water Trap (UDI 04719894384061)

Manufactured by VADI Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reusable Water Trap - Primary ID 04719894384061

Device Regulatory Overview

The Reusable Water Trap (Model/Catalog Number: G-313003-2-0-HM) is a medical device manufactured by VADI Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R028003 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
G-313003-2-0-HM
Product Code / EMDN
R028003
Device Name
Reusable Water Trap
Database Sync Date
2026-08-09 16:28:51

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Reusable Water Trap?

The registered manufacturer of record for Reusable Water Trap is VADI Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for Reusable Water Trap?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719894384061.

What classification code is assigned to this device?

This device is registered under product classification code R028003.

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