GUDIDData
eudamed_udi Primary ID: 56947793304559

Hollow Fiber Dialyzer (UDI 56947793304559)

Manufactured by Shandong Weigao Blood Purification Products Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hollow Fiber Dialyzer - Primary ID 56947793304559

Device Regulatory Overview

The Hollow Fiber Dialyzer (Model/Catalog Number: TCG0121) is a medical device manufactured by Shandong Weigao Blood Purification Products 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
TCG0121
Product Code / EMDN
F01060303
Device Name
Hollow Fiber Dialyzer
Database Sync Date
2026-08-09 16:48:37

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Hollow Fiber Dialyzer?

The registered manufacturer of record for Hollow Fiber Dialyzer is Shandong Weigao Blood Purification Products Co., Ltd..

What is the Primary UDI-DI identifier for Hollow Fiber Dialyzer?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 56947793304559.

What classification code is assigned to this device?

This device is registered under product classification code F01060303.

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