GUDIDData
eudamed_udi Primary ID: 06978896415236

Vitamin D Test Kit (Immunofluorescence Method) (UDI 06978896415236)

Manufactured by WUHAN EASYDIAGNOSIS BIOMEDICINE CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vitamin D Test Kit (Immunofluorescence Method) - Primary ID 06978896415236

Device Regulatory Overview

The Vitamin D Test Kit (Immunofluorescence Method) (Model/Catalog Number: W-IF-VD-40) is a medical device manufactured by WUHAN EASYDIAGNOSIS BIOMEDICINE CO., LTD.. This product is indexed under FDA Product Code / Category Classification W0102060309 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
W-IF-VD-40
Product Code / EMDN
W0102060309
Device Name
Vitamin D Test Kit (Immunofluorescence Method)
Database Sync Date
2026-08-09 16:46:20

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 Vitamin D Test Kit (Immunofluorescence Method)?

The registered manufacturer of record for Vitamin D Test Kit (Immunofluorescence Method) is WUHAN EASYDIAGNOSIS BIOMEDICINE CO., LTD..

What is the Primary UDI-DI identifier for Vitamin D Test Kit (Immunofluorescence Method)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978896415236.

What classification code is assigned to this device?

This device is registered under product classification code W0102060309.

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