Jiekang (UDI YJK-F1)

Manufactured by Zhangjiagang Jiekang Medical Devices Equipment Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Jiekang (Model/Catalog Number: YJK-F1) is a medical device manufactured by Zhangjiagang Jiekang Medical Devices Equipment Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification FPP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: YJK-F1
Product Code / EMDN: FPP
Device Name
Database Sync Date: 2026-08-09 09:06:36

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 Jiekang?

The registered manufacturer of record for Jiekang is Zhangjiagang Jiekang Medical Devices Equipment Co.,Ltd..

What is the Primary UDI-DI identifier for Jiekang?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is YJK-F1.

What classification code is assigned to this device?

This device is registered under product classification code FPP.

Similar Classification Devices (FPP)

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