iCruise (UDI 11952)

Manufactured by XIAMEN TAFT MEDICAL CO.,LTD.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The iCruise (Model/Catalog Number: 11952) is a medical device manufactured by XIAMEN TAFT MEDICAL CO.,LTD.. This product is indexed under FDA Product Code / Category Classification IOR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 11952
Product Code / EMDN: IOR
Device Name
Database Sync Date: 2026-08-09 09:06:41

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 iCruise?

The registered manufacturer of record for iCruise is XIAMEN TAFT MEDICAL CO.,LTD..

What is the Primary UDI-DI identifier for iCruise?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11952.

What classification code is assigned to this device?

This device is registered under product classification code IOR.

Similar Classification Devices (IOR)

Other Devices by XIAMEN TAFT MEDICAL CO.,LTD.

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