gudid
Primary ID: U82RH
VIETWELL HOME CARE (UDI U82RH)
Manufactured by Shenzhen Urion Technology Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIETWELL HOME CARE - Primary ID U82RH
Device Regulatory Overview
The VIETWELL HOME CARE (Model/Catalog Number: U82RH) is a medical device manufactured by Shenzhen Urion Technology Co., Ltd. This product is indexed under FDA Product Code / Category Classification DXN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- U82RH
- Product Code / EMDN
- DXN
- Device Name
- Database Sync Date
- 2026-08-09 09:05:25
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 VIETWELL HOME CARE?
The registered manufacturer of record for VIETWELL HOME CARE is Shenzhen Urion Technology Co., Ltd.
What is the Primary UDI-DI identifier for VIETWELL HOME CARE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is U82RH.
What classification code is assigned to this device?
This device is registered under product classification code DXN.
Similar Classification Devices (DXN)
Other Devices by Shenzhen Urion Technology Co., Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint