eudamed_udi Primary ID: 06971674865025

Calcium (Ca) Test Kit (Arsenazo Ⅲ) (UDI 06971674865025)

Manufactured by Biobase Biodustry(Shandong) Co.,Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Calcium (Ca) Test Kit (Arsenazo Ⅲ) (Model/Catalog Number: R:40mL×4（716）) is a medical device manufactured by Biobase Biodustry(Shandong) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W01010303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: R:40mL×4（716）
Product Code / EMDN: W01010303
Device Name: Calcium (Ca) Test Kit (Arsenazo Ⅲ)
Database Sync Date: 2026-08-09 16:28:59

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Calcium (Ca) Test Kit (Arsenazo Ⅲ)?

The registered manufacturer of record for Calcium (Ca) Test Kit (Arsenazo Ⅲ) is Biobase Biodustry(Shandong) Co.,Ltd..

What is the Primary UDI-DI identifier for Calcium (Ca) Test Kit (Arsenazo Ⅲ)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971674865025.

What classification code is assigned to this device?

This device is registered under product classification code W01010303.

Similar Classification Devices (W01010303)

Other Devices by Biobase Biodustry(Shandong) Co.,Ltd.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint