eudamed_udi Primary ID: 06954414743944

Insulin Fast Test Kit (Immunofluorescence Assay) (UDI 06954414743944)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Insulin Fast Test Kit (Immunofluorescence Assay) (Model/Catalog Number: IF5146) is a medical device manufactured by Getein Biotech, Inc.. This product is indexed under FDA Product Code / Category Classification W0102060103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: IF5146
Product Code / EMDN: W0102060103
Device Name: Insulin Fast Test Kit (Immunofluorescence Assay)
Database Sync Date: 2026-08-09 17:40:30

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 Insulin Fast Test Kit (Immunofluorescence Assay)?

The registered manufacturer of record for Insulin Fast Test Kit (Immunofluorescence Assay) is Getein Biotech, Inc..

What is the Primary UDI-DI identifier for Insulin Fast Test Kit (Immunofluorescence Assay)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06954414743944.

What classification code is assigned to this device?

This device is registered under product classification code W0102060103.

Similar Classification Devices (W0102060103)

Other Devices by Getein Biotech, Inc.

Programmatic Export

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

JSON API Endpoint