eudamed_udi Primary ID: 08051887043156

THD N-ANO BASIC MAXI (BE) (UDI 08051887043156)

Manufactured by THD S.P.A.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The THD N-ANO BASIC MAXI (BE) (Model/Catalog Number: 800304) is a medical device manufactured by THD S.P.A.. This product is indexed under FDA Product Code / Category Classification G02060301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 800304
Product Code / EMDN: G02060301
Device Name: THD Not Sterile AnoProctoRectoscopes LED and not LED
Database Sync Date: 2026-08-09 16:28:45

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 THD N-ANO BASIC MAXI (BE)?

The registered manufacturer of record for THD N-ANO BASIC MAXI (BE) is THD S.P.A..

What is the Primary UDI-DI identifier for THD N-ANO BASIC MAXI (BE)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051887043156.

What classification code is assigned to this device?

This device is registered under product classification code G02060301.

Similar Classification Devices (G02060301)

Other Devices by THD S.P.A.

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