gudid Primary ID: XW-PTB-8S

VU (UDI XW-PTB-8S)

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: XW-PTB-8S) is a medical device manufactured by Xiamen Weiyou Intelligent Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FNL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: XW-PTB-8S
Product Code / EMDN: FNL
Device Name: Medical parallel transport bed
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 XW-PTB-8S.

What classification code is assigned to this device?

This device is registered under product classification code FNL.

Similar Classification Devices (FNL)

Other Devices by Xiamen Weiyou Intelligent Technology Co.,Ltd

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