GUDIDData
eudamed_udi Primary ID: 06976560481761

Sodium Fluoride / EDTA.Na2 (Glucose Tube)2ml (UDI 06976560481761)

Manufactured by Jiangxi Exquisite Technology Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sodium Fluoride / EDTA.Na2 (Glucose Tube)2ml - Primary ID 06976560481761

Device Regulatory Overview

The Sodium Fluoride / EDTA.Na2 (Glucose Tube)2ml (Model/Catalog Number: B01SF002) is a medical device manufactured by Jiangxi Exquisite Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W050101010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
B01SF002
Product Code / EMDN
W050101010201
Device Name
Blood Collection Tube For Single-Use
Database Sync Date
2026-08-09 16:52:03

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 Sodium Fluoride / EDTA.Na2 (Glucose Tube)2ml?

The registered manufacturer of record for Sodium Fluoride / EDTA.Na2 (Glucose Tube)2ml is Jiangxi Exquisite Technology Co.,Ltd..

What is the Primary UDI-DI identifier for Sodium Fluoride / EDTA.Na2 (Glucose Tube)2ml?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976560481761.

What classification code is assigned to this device?

This device is registered under product classification code W050101010201.

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