eudamed_udi Primary ID: 05425023688175

DIASpot Neptune Connectivitis 10 IgG (UDI 05425023688175)

Manufactured by D-tek s.a.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The DIASpot Neptune Connectivitis 10 IgG (Model/Catalog Number: KAPDTCT10N) is a medical device manufactured by D-tek s.a.. This product is indexed under FDA Product Code / Category Classification W0102100101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: KAPDTCT10N
Product Code / EMDN: W0102100101
Device Name: BlueDiver Dot ANA Screening
Database Sync Date: 2026-08-09 16:51:44

Full Regulatory Attributes

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

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Frequently Asked Questions

Who is the primary manufacturer of DIASpot Neptune Connectivitis 10 IgG?

The registered manufacturer of record for DIASpot Neptune Connectivitis 10 IgG is D-tek s.a..

What is the Primary UDI-DI identifier for DIASpot Neptune Connectivitis 10 IgG?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05425023688175.

What classification code is assigned to this device?

This device is registered under product classification code W0102100101.

Similar Classification Devices (W0102100101)

Other Devices by D-tek s.a.

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