GUDIDData
gudid Primary ID: Truncated Proctoscope Medium Sterile

THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (UDI Truncated Proctoscope Medium Sterile)

Manufactured by THD SPA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope - Primary ID Truncated Proctoscope Medium Sterile

Device Regulatory Overview

The THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (Model/Catalog Number: Truncated Proctoscope Medium Sterile) is a medical device manufactured by THD SPA. This product is indexed under FDA Product Code / Category Classification GCP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Truncated Proctoscope Medium Sterile
Product Code / EMDN
GCP
Device Name
The THD proctoscope is a disposable medical device deemed for examination and treatment of the anal and rectum Available with truncated or beveled tip.
Database Sync Date
2026-08-09 09:04:34

Full Regulatory Attributes

🔒 Token Gated
{
    "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 disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope?

The registered manufacturer of record for THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope is THD SPA.

What is the Primary UDI-DI identifier for THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Truncated Proctoscope Medium Sterile.

What classification code is assigned to this device?

This device is registered under product classification code GCP.

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