GUDIDData
eudamed_udi Primary ID: 69743840303186

FOB Rapid Test (UDI 69743840303186)

Manufactured by Zhejiang Anji Saianfu Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FOB Rapid Test - Primary ID 69743840303186

Device Regulatory Overview

The FOB Rapid Test (Model/Catalog Number: 3040101) is a medical device manufactured by Zhejiang Anji Saianfu Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102039013 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
3040101
Product Code / EMDN
W0102039013
Device Name
FOB Rapid Test
Database Sync Date
2026-08-09 16:30:10

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 FOB Rapid Test?

The registered manufacturer of record for FOB Rapid Test is Zhejiang Anji Saianfu Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for FOB Rapid Test?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 69743840303186.

What classification code is assigned to this device?

This device is registered under product classification code W0102039013.

Programmatic Export

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

JSON API Endpoint