GUDIDData
eudamed_udi Primary ID: 06958982140235

Rotavirus Ag Test (UDI 06958982140235)

Manufactured by Abiores Technology (Beijing) Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rotavirus Ag Test - Primary ID 06958982140235

Device Regulatory Overview

The Rotavirus Ag Test (Model/Catalog Number: AH40-20) is a medical device manufactured by Abiores Technology (Beijing) Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0105099099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AH40-20
Product Code / EMDN
W0105099099
Device Name
Rotavirus Ag Test
Database Sync Date
2026-08-09 17:31:32

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 Rotavirus Ag Test?

The registered manufacturer of record for Rotavirus Ag Test is Abiores Technology (Beijing) Co.,Ltd..

What is the Primary UDI-DI identifier for Rotavirus Ag Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958982140235.

What classification code is assigned to this device?

This device is registered under product classification code W0105099099.

Programmatic Export

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

JSON API Endpoint