gudid Primary ID: Anoscope N-Ano MAXI Truncated

THD N-ano anoscope (UDI Anoscope N-Ano MAXI Truncated)

Manufactured by THD SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The THD N-ano anoscope (Model/Catalog Number: Anoscope N-Ano MAXI Truncated) is a medical device manufactured by THD SPA. This product is indexed under FDA Product Code / Category Classification FER within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Anoscope N-Ano MAXI Truncated
Product Code / EMDN: FER
Device Name: The THD N-ano anoscope is a disposable medical device deemed for investigation of the anal canal.The THD N-ano anoscope combines in a single device a light anoscope and a powerful, fully integrated, LED light source, in order to have a clear and detailed vision of the inspection field.The THD N-ano anoscope is ready-to-use and does not need for other tools.
Database Sync Date: 2026-08-09 09:04:34

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 anoscope?

The registered manufacturer of record for THD N-ano anoscope is THD SPA.

What is the Primary UDI-DI identifier for THD N-ano anoscope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Anoscope N-Ano MAXI Truncated.

What classification code is assigned to this device?

This device is registered under product classification code FER.

Similar Classification Devices (FER)

Other Devices by THD SPA

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