gudid Primary ID: VU-IPC12C

VU (UDI VU-IPC12C)

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-IPC12C) 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-IPC12C
Product Code / EMDN: IRP
Device Name: Air Pressure Therapy System
Database Sync Date: 2026-08-09 09:06:44

Full Regulatory Attributes

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{
    "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 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-IPC12C.

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

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