eudamed_udi Primary ID: 04066418100059

FX 600 (UDI 04066418100059)

Manufactured by Fresenius Medical Care (Jiangsu) Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The FX 600 (Model/Catalog Number: CN0684) is a medical device manufactured by Fresenius Medical Care (Jiangsu) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification F01060303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CN0684
Product Code / EMDN: F01060303
Device Name: FX class dialyzers
Database Sync Date: 2026-08-09 16:50:16

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 FX 600?

The registered manufacturer of record for FX 600 is Fresenius Medical Care (Jiangsu) Co., Ltd..

What is the Primary UDI-DI identifier for FX 600?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04066418100059.

What classification code is assigned to this device?

This device is registered under product classification code F01060303.

Similar Classification Devices (F01060303)

Other Devices by Fresenius Medical Care (Jiangsu) Co., Ltd.

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