GUDIDData
eudamed_udi Primary ID: 06952062773269

H.Pylori Antibody Test Kit (UDI 06952062773269)

Manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for H.Pylori Antibody Test Kit - Primary ID 06952062773269

Device Regulatory Overview

The H.Pylori Antibody Test Kit (Model/Catalog Number: HPAb2W-10) is a medical device manufactured by ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD. This product is indexed under FDA Product Code / Category Classification W0105010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HPAb2W-10
Product Code / EMDN
W0105010402
Device Name
H.Pylori Antibody Test Kit
Database Sync Date
2026-08-09 16:29:31

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 H.Pylori Antibody Test Kit?

The registered manufacturer of record for H.Pylori Antibody Test Kit is ANHUI DEEPBLUE MEDICAL TECHNOLOGY CO.,LTD.

What is the Primary UDI-DI identifier for H.Pylori Antibody Test Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06952062773269.

What classification code is assigned to this device?

This device is registered under product classification code W0105010402.

Programmatic Export

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

JSON API Endpoint