gudid Primary ID: VU-IPC04B

VU (UDI VU-IPC04B)

Manufactured by Xiamen Weiyou Intelligent Technology Co.,Ltd

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The VU (Model/Catalog Number: VU-IPC04B) is a medical device manufactured by Xiamen Weiyou Intelligent Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification IRP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: VU-IPC04B
Product Code / EMDN: IRP
Device Name: Air Pressure Therapy System
Database Sync Date: 2026-08-09 09:06:44

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 VU?

The registered manufacturer of record for VU is Xiamen Weiyou Intelligent Technology Co.,Ltd.

What is the Primary UDI-DI identifier for VU?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VU-IPC04B.

What classification code is assigned to this device?

This device is registered under product classification code IRP.

Similar Classification Devices (IRP)

Other Devices by Xiamen Weiyou Intelligent Technology Co.,Ltd

Programmatic Export

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

JSON API Endpoint