eudamed_udi Primary ID: 04250289510745

AESKUBLOTS® Food Intolerance FIVE (UDI 04250289510745)

Manufactured by Aesku.Diagnostics GmbH & Co. KG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The AESKUBLOTS® Food Intolerance FIVE (Model/Catalog Number: 431405) is a medical device manufactured by Aesku.Diagnostics GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification W0102010106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 431405
Product Code / EMDN: W0102010106
Device Name: AESKUBLOTS® Food Intolerance
Database Sync Date: 2026-08-09 16:48:24

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 AESKUBLOTS® Food Intolerance FIVE?

The registered manufacturer of record for AESKUBLOTS® Food Intolerance FIVE is Aesku.Diagnostics GmbH & Co. KG.

What is the Primary UDI-DI identifier for AESKUBLOTS® Food Intolerance FIVE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250289510745.

What classification code is assigned to this device?

This device is registered under product classification code W0102010106.

Similar Classification Devices (W0102010106)

Other Devices by Aesku.Diagnostics GmbH & Co. KG

Programmatic Export

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

JSON API Endpoint