GUDIDData
gudid Primary ID: THD Light - Scope Rectoscope Medium Sterile

THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (UDI THD Light - Scope Rectoscope 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 THD Light - Scope Rectoscope Medium Sterile

Device Regulatory Overview

The THD disposable sterile and not sterie Ano-, Procto- Rectoscopes and Light-scope (Model/Catalog Number: THD Light - Scope Rectoscope Medium Sterile) 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
THD Light - Scope Rectoscope Medium Sterile
Product Code / EMDN
FER
Device Name
The THD Light-Scope rectoscope is a disposable medical device deemed for investigation of the anal canal and of the distal region of the sigma. The THD Light-Scope rectoscope combines a magnifier lens in the back cap. The handle has a lodgement for a THD Fiber Optic Cable tip for using the rectoscope with a THD light source. The THD Light-Scope rectoscope is ready-to-use and can also be available with an inflation bulb included.
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
}
                            

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 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 THD Light - Scope Rectoscope Medium Sterile.

What classification code is assigned to this device?

This device is registered under product classification code FER.

Programmatic Export

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

JSON API Endpoint