eudamed_udi Primary ID: 04262435350051

Unspecified Brand (UDI 04262435350051)

Manufactured by TCC GmbH

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: MD008) is a medical device manufactured by TCC GmbH. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MD008
Product Code / EMDN: V92
Device Name: Sepsis Prediction Service
Database Sync Date: 2026-08-09 16:29:38

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is TCC GmbH.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262435350051.

What classification code is assigned to this device?

This device is registered under product classification code V92.

Similar Classification Devices (V92)

Other Devices by TCC GmbH

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