eudamed_udi Primary ID: 06975550990139

Unspecified Brand (UDI 06975550990139)

Manufactured by Cangzhou Fukang Medical Supplies Co.,Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: Sodium Fluoride (EDTA) Tube) is a medical device manufactured by Cangzhou Fukang Medical Supplies Co.,Ltd. This product is indexed under FDA Product Code / Category Classification W050101010202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Sodium Fluoride (EDTA) Tube
Product Code / EMDN: W050101010202
Device Name: Non Vacuum Blood Collection Tube
Database Sync Date: 2026-08-09 16:28:57

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Cangzhou Fukang Medical Supplies Co.,Ltd.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975550990139.

What classification code is assigned to this device?

This device is registered under product classification code W050101010202.

Similar Classification Devices (W050101010202)

Other Devices by Cangzhou Fukang Medical Supplies Co.,Ltd

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