IF (UDI YFWB-63)

Manufactured by IF Health (Xiamen) Intelligent Technology Co.,Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The IF (Model/Catalog Number: YFWB-63) is a medical device manufactured by IF Health (Xiamen) Intelligent Technology Co.,Ltd. This product is indexed under FDA Product Code / Category Classification ITI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: YFWB-63
Product Code / EMDN: ITI
Device Name
Database Sync Date: 2026-08-09 09:06:39

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 IF?

The registered manufacturer of record for IF is IF Health (Xiamen) Intelligent Technology Co.,Ltd.

What is the Primary UDI-DI identifier for IF?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is YFWB-63.

What classification code is assigned to this device?

This device is registered under product classification code ITI.

Similar Classification Devices (ITI)

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